Composition for organic electronic devices

ABSTRACT

The present invention relates to a composition which comprises an electron-transporting host and a hole-transporting host, to the use thereof in electronic devices and to electronic devices containing this composition. The electron-transporting host is particularly preferably selected from the class of the lactams. The hole-transporting host is preferably selected from the class of the biscarbazoles.

The present invention relates to a composition which comprises an electron-transporting host and a hole-transporting host, to the use thereof in electronic devices and to electronic devices containing this composition. The electron-transporting host is particularly preferably selected from the class of the lactams. The hole-transporting host is preferably selected from the class of the biscarbazoles.

The structure of organic electroluminescent devices (for example OLEDs—organic light-emitting diodes, or OLECs—organic light-emitting electrochemical cells) in which organic semiconductors are employed as functional materials is described, for example, in U.S. Pat. Nos. 4,539,507, 5,151,629, EP 0676461 and WO 98/27136. The emitting materials employed here, besides fluorescent emitters, are increasingly organometallic complexes which exhibit phosphorescence instead of fluorescence (M. A. Baldo et al., Appl. Phys. Lett. 1999, 75, 4-6). For quantum-mechanical reasons, an up to four-fold increase in energy and power efficiency is possible using organometallic compounds as phosphorescence emitters. In general, however, there is still a need for improvement, for example with respect to efficiency, operating voltage and lifetime, in the case of OLEDs, in particular also in the case of OLEDs which exhibit triplet emission (phosphorescence).

The properties of organic electroluminescent devices are not determined only by the emitters employed. Of particular importance here are also, in particular, the other materials used, such as host and matrix materials, hole-blocking materials, electron-transport materials, hole-transport materials and electron- or exciton-blocking materials, and of these in particular the host or matrix materials. Improvements in these materials can result in significant improvements in electroluminescent devices.

Host materials for use in organic electronic devices are well known to the person skilled in the art. The term matrix material is frequently also used in the prior art to mean a host material for phosphorescent emitters. This use of the term also applies to the present invention. In the meantime, a multiplicity of host materials have been developed, both for fluorescent and for phosphorescent electronic devices.

According to the prior art, use is made, inter alia, of ketones (for example in accordance with WO 2004/093207 or WO 2010/006680) or phosphine oxides (for example in accordance with WO 2005/003253) as matrix materials for phosphorescent emitters. Further matrix materials in accordance with the prior art are triazines (for example WO 2008/056746, EP 0906947, EP 0908787, EP 0906948) and lactams (for example WO 2011/137951). Furthermore, use is made in accordance with the prior art of, inter alia, carbazole derivatives (for example in accordance with WO 2005/039246, US 2005/0069729 or WO 2014/015931), indolocarbazole derivatives (for example in accordance with WO 2007/063754 or WO 2008/056746) or indenocarbazole derivatives (for example in accordance with WO 2010/136109 or WO 2011/000455), in particular those which are substituted by electron-deficient heteroaromatic groups, such as triazine, as matrix materials for phosphorescent emitters. WO 2011/057706 discloses carbazole derivatives which are substituted by two triphenyltriazine groups. WO 2011/046182 discloses carbazol-arylene-triazine derivatives which are substituted on the triazine by a fluorenyl group. WO 2009/069442 discloses tricyclic compounds, such as carbazole, dibenzofuran or dibenzothiophene, which are substituted to a high degree by electron-deficient heteroaromatic groups (for example pyridine, pyrimidine or triazine), as host materials. WO 2011/057706 and WO 2015/169412 disclose further host materials which comprise, inter alia, triazine-dibenzofuran-carbazole derivatives and triazine-dibenzothiophene-carbazole derivatives.

A further possibility for improving the performance data of electronic devices, in particular of organic electroluminescent devices, consists in using combinations of two or more materials, in particular host materials or matrix materials.

U.S. Pat. No. 6,392,250 B1 discloses the use of a mixture consisting of an electron-transport material, a hole-transport material and a fluorescent emitter in the emission layer of an OLED. With the aid of this mixture, it has been possible to improve the lifetime of the OLED compared with the prior art.

U.S. Pat. No. 6,803,720 B1 discloses the use of a mixture comprising a phosphorescent emitter and a hole-transport material and an electron-transport material in the emission layer of an OLED. Both the hole-transport material and the electron-transport material are small organic molecules.

According to WO 2011/137951, lactams can be used in a mixture, for example together with triazine derivatives.

According to WO 2013/064206, lactams can be used in a mixture with, for example, a biscarbazole of the formula

According to WO 2014/094964, lactams can be used in a mixture with a biscarbazole of the formula

However, there is still a need for improvement, in particular in relation to the lifetime of the organic electronic device, on use of these materials or on use of mixtures of the materials.

The object of the present invention is therefore the provision of materials which are suitable for use in an organic electronic device, in particular in an organic electroluminescent device, and in particular in a fluorescent or phosphorescent OLED, and lead to good device properties, in particular with respect to an improved lifetime, and the provision of the corresponding electronic device.

It is now been found that compositions which comprise compounds of the formula (1) and a hole-transporting host of the formula (2), preferably biscarbazoles, achieve this object and overcome the disadvantages from the prior art, in particular the disadvantages from the prior art WO 2013/064206 and WO 2014/094964. Compositions of this type lead to very good properties of organic electronic devices, in particular organic electroluminescent devices, in particular with respect to the lifetime and in particular also in the presence of a light-emitting component in the emission layer at concentrations between 2 and 15% by weight.

The present invention therefore relates firstly to a composition comprising at least one compound of the formula (1) and at least one compound of the formula (2)

-   where the following applies to the symbols and indices used: -   X is on each occurrence, identically or differently, CR or N; -   V is a bond: C(R⁰)₂, NR, O or S; -   v is 0 or 1; -   X₂ is on each occurrence, identically or differently, CR¹ or N; -   Z is C(R⁰)₂, NR¹, O or S; -   n is 0 or 1; -   Ar₁ and Ar₂ are in each case, independently of one another, an     aromatic ring system having 6 to 40 aromatic ring atoms or a     heteroaromatic ring system having 10 to 40 aromatic ring atoms,     which may be substituted by one or more radicals R³; -   R⁰ is on each occurrence, identically or differently, a     straight-chain or branched alkyl group having 1 to 4 C atoms or both     R⁰ form a monocyclic or polycyclic, aliphatic, aromatic or     heteroaromatic ring system, which may be substituted by one or more     radicals R²; -   R is selected on each occurrence, identically or differently, from     the group consisting of H, D, F, Cl, Br, I, CN, NO₂, N(Ar)₂, N(R²)₂,     C(═O)Ar, C(═O)R², P(═O)(Ar)₂, P(Ar)₂, B(Ar)₂, Si(Ar)₃, Si(R²)₃, a     straight-chain alkyl, alkoxy or thioalkyl group having 1 to 20 C     atoms or a branched or cyclic alkyl, alkoxy or thioalkyl group     having 3 to 20 C atoms or an alkenyl group having 2 to 20 C atoms,     which may in each case be substituted by one or more radicals R²,     where one or more non-adjacent CH₂ groups may be replaced by     R²C═CR², Si(R²)₂, C═O, C═S, C═NR², P(═O)(R²), SO, SO₂, NR², O, S or     CONR² and where one or more H atoms may be replaced by D, F, Cl, Br,     I, CN or NO₂, an aromatic or heteroaromatic ring system having 5 to     40 aromatic ring atoms, which may in each case be substituted by one     or more radicals R², or an aryloxy or heteroaryloxy group having 5     to 40 aromatic ring atoms, which may be substituted by one or more     radicals R², or an aralkyl or heteroaralkyl group having 5 to 40     aromatic ring atoms, which may be substituted by one or more     radicals R²; two substituents R which are bonded to the same carbon     atom or to adjacent carbon atoms may optionally form a monocyclic or     polycyclic, aliphatic, aromatic or heteroaromatic ring system, which     may be substituted by one or more radicals R²; -   R¹ is selected on each occurrence, identically or differently, from     the group consisting of H, D, F, Cl, Br, I, CN, NO₂, N(Ar)₂, N(R²)₂,     C(═O)Ar, C(═O)R², P(═O)(Ar)₂, P(Ar)₂, B(Ar)₂, Si(Ar)₃, Si(R²)₃, a     straight-chain alkyl, alkoxy or thioalkyl group having 1 to 20 C     atoms or a branched or cyclic alkyl, alkoxy or thioalkyl group     having 3 to 20 C atoms or an alkenyl group having 2 to 20 C atoms,     which may in each case be substituted by one or more radicals R²,     where one or more non-adjacent CH₂ groups may be replaced by     R²C═CR², Si(R²)₂, C═O, C═S, C═NR², P(═O)(R²), SO, SO₂, NR², O, S or     CONR² and where one or more H atoms may be replaced by D, F, Cl, Br,     I, CN or NO₂, an aromatic or heteroaromatic ring system having 5 to     40 aromatic ring atoms, which may in each case be substituted by one     or more radicals R², or an aryloxy or heteroaryloxy group having 5     to 40 aromatic ring atoms, which may be substituted by one or more     radicals R², or an aralkyl or heteroaralkyl group having 5 to 40     aromatic ring atoms, which may be substituted by one or more     radicals R²; -   R² is selected on each occurrence, identically or differently, from     the group consisting of H, D, F, Cl, Br, I, CN, NO₂, N(Ar)₂, NH₂,     N(R³)₂, C(═O)Ar, C(═O)H, C(═O)R³, P(═O)(Ar)₂, a straight-chain     alkyl, alkoxy or thioalkyl group having 1 to 40 C atoms or a     branched or cyclic alkyl, alkoxy or thioalkyl group having 3 to 40 C     atoms or an alkenyl or alkynyl group having 2 to 40 C atoms, which     may in each case be substituted by one or more radicals R³, where     one or more non-adjacent CH₂ groups may be replaced by HC═CH,     R³C═CR³, C═C, Si(R³)₂, Ge(R³)₂, Sn(R³)₂, C═O, C═S, C═Se, C═NR³,     P(═O)(R³), SO, SO₂, NH, NR³, O, S, CONH or CONR³ and where one or     more H atoms may be replaced by D, F, Cl, Br, I, CN or NO₂, an     aromatic or heteroaromatic ring system having 5 to 60 aromatic ring     atoms, which may in each case be substituted by one or more radicals     R³, or an aryloxy or heteroaryloxy group having 5 to 60 aromatic     ring atoms, which may be substituted by one or more radicals R³, or     a combination of these systems, where two or more adjacent     substituents R² may optionally form a monocyclic or polycyclic,     aliphatic, aromatic or heteroaromatic ring system, which may be     substituted by one or more radicals R³; -   R³ is selected on each occurrence, identically or differently, from     the group consisting of H, D, F, CN, an aliphatic hydrocarbon     radical having 1 to 20 C atoms or an aromatic ring system having 6     to 30 ring atoms or a heteroaromatic ring system having 10 to 30     ring atoms, in which one or more H atoms may be replaced by D, F,     Cl, Br, I or CN and which may be substituted by one or more alkyl     groups, each having 1 to 4 carbon atoms; two or more adjacent     substituents R³ may form a mono- or polycyclic, aliphatic ring     system with one another; -   Ar is on each occurrence, identically or differently, an aromatic or     heteroaromatic ring system having 5 to 30 aromatic ring atoms, which     may be substituted by one or more non-aromatic radicals R³; two     radicals Ar which are bonded to the same N atom, P atom or B atom     may also be bridged to one another by a single bond or a bridge     selected from N(R³), C(R³)₂, O or S.

The invention furthermore relates to formulations which comprise compositions of this type, to the use of these compositions in an organic electronic device, to organic electronic devices, preferably electroluminescent devices, which contain compositions of this type, and preferably contain the composition in a layer, and to a process for the production of devices of this type. The present invention likewise relates to the corresponding preferred embodiments, as described below. The surprising and advantageous effects are achieved by specific selection of known materials, in particular relating to the choice of the hole-transporting materials of the formula (2).

The layer which comprises the composition comprising at least one compound of the formula (1) and at least one compound of the formula (2), as described above or preferably described below, is, in particular, an emitting layer (EML), an electron-transport layer (ETL), an electron-injection layer (EIL) and/or a hole-blocking layer (HBL).

In the case of an emitting layer, this is preferably a phosphorescent layer which is characterised in that it comprises a phosphorescent emitter in addition to the composition comprising the matrix materials of the formula (1) and formula (2), as described above.

Adjacent carbon atoms in the sense of the present invention are carbon atoms which are linked directly to one another.

The formulation that two or more radicals can form a ring with one another is, for the purposes of the present description, intended to be taken to mean, inter alia, that the two radicals are linked to one another by a chemical bond with formal elimination of two hydrogen atoms. This is illustrated by the following scheme:

Furthermore, however, the above-mentioned formulation is also intended to be taken to mean that, in the case where one of the two radicals represents hydrogen, the second radical is bonded at the position at which the hydrogen atom was bonded, with formation of a ring. This is intended to be illustrated by the following scheme:

An aryl group in the sense of this invention contains 6 to 40 aromatic ring atoms, preferably C atoms. A heteroaryl group in the sense of this invention contains 5 to 40 aromatic ring atoms, where the ring atoms include C atoms and at least one heteroatom, with the proviso that the sum of C atoms and heteroatoms is at least 5. The heteroatoms are preferably selected from N, O and/or S. An aryl group or heteroaryl group here is either a simple aromatic ring, i.e. phenyl, derived from benzene, or a simple heteroaromatic ring, for example derived from pyridine, pyrimidine or thiophene, or a condensed aryl or heteroaryl group, for example naphthalene, anthracene, phenanthrene, quinoline or isoquinoline.

An aromatic ring system in the sense of this invention contains 6 to 40 C atoms in the ring system and may be substituted by one or more radicals R³, where R³ has a meaning described below. An aromatic ring system also contains aryl groups, as described above.

A heteroaromatic ring system in the sense of this invention contains 5 to 40 ring atoms and at least one heteroatom and may be substituted by one or more radicals R³, where R³ has a meaning described below. A preferred heteroaromatic ring system has 10 to 40 ring atoms and at least one heteroatom and may be substituted by one or more radicals R³, where R³ has a meaning described below. A heteroaromatic ring system also contains heteroaryl groups, as described above. The heteroatoms in the heteroaromatic ring system are preferably selected from N, O and/or S.

An aromatic or heteroaromatic ring system in the sense of this invention is taken to mean a system which does not necessarily contain only aryl or heteroaryl groups, but instead in which, in addition, a plurality of aryl or heteroaryl groups may be interrupted by a non-aromatic unit (preferably less than 10% of the atoms other than H), such as, for example, a C, N or O atom or a carbonyl group. Thus, for example, systems such as 9,9′-spirobifluorene, 9,9-diarylfluorene, triarylamine, diaryl ether, stilbene, etc. are intended to be taken to be aromatic or heteroaromatic ring systems in the sense of this invention, as are systems in which two or more aryl groups are interrupted, for example, by a linear or cyclic alkyl group or by a silyl group. Furthermore, systems in which two or more aryl or heteroaryl groups are bonded directly to one another, such as, for example, biphenyl, terphenyl, quaterphenyl or bipyridine, are likewise covered by the definition of the aromatic or heteroaromatic ring system.

An aromatic or heteroaromatic ring system having 5-40 aromatic ring atoms, which may also in each case be substituted by the said radicals R³ and which may be linked to the aromatic or heteroaromatic ring system via any desired positions, is taken to mean, for example, groups derived from benzene, naphthalene, anthracene, benzanthracene, phenanthrene, benzophenanthrene, pyrene, chrysene, perylene, fluoranthene, benzofluoranthene, naphthacene, pentacene, benzopyrene, biphenyl, biphenylene, terphenyl, terphenylene, fluorene, spirobifluorene, dihydrophenanthrene, dihydropyrene, tetrahydropyrene, cis- or trans-indenofluorene, cis- or transmonobenzoindenofluorene, cis- or trans-dibenzoindenofluorene, truxene, isotruxene, spirotruxene, spiroisotruxene, furan, benzofuran, isobenzofuran, dibenzofuran, thiophene, benzothiophene, isobenzothiophene, dibenzothiophene, pyrrole, indole, isoindole, carbazole, indolocarbazole, indenocarbazole, pyridine, quinoline, isoquinoline, acridine, phenanthridine, benzo-5,6-quinoline, benzo-6,7-quinoline, benzo-7,8-quinoline, phenothiazine, phenoxazine, pyrazole, indazole, imidazole, benzimidazole, naphthimidazole, phenanthrimidazole, pyridimidazole, pyrazinimidazole, quinoxalinimidazole, oxazole, benzoxazole, naphthoxazole, anthroxazole, phenanthroxazole, isoxazole, 1,2-thiazole, 1,3-thiazole, benzothiazole, pyridazine, benzopyridazine, pyrimidine, benzopyrimidine, quinoxaline, 1,5-diazaanthracene, 2,7-diazapyrene, 2,3-diazapyrene, 1,6-diazapyrene, 1,8-diazapyrene, 4,5-diazapyrene, 4,5,9,10-tetraazaperylene, pyrazine, phenazine, phenoxazine, phenothiazine, fluorubin, naphthyridine, azacarbazole, benzocarboline, phenanthroline, 1,2,3-triazole, 1,2,4-triazole, benzotriazole, 1,2,3-oxadiazole, 1,2,4-oxadiazole, 1,2,5-oxadiazole, 1,3,4-oxadiazole, 1,2,3-thiadiazole, 1,2,4-thiadiazole, 1,2,5-thiadiazole, 1,3,4-thiadiazole, 1,3,5-triazine, 1,2,4-triazine, 1,2,3-triazine, tetrazole, 1,2,4,5-tetrazine, 1,2,3,4-tetrazine, 1,2,3,5-tetrazine, purine, pteridine, indolizine and benzothiadiazole.

The abbreviation Ar is on each occurrence, identically or differently, an aromatic or heteroaromatic ring system having 5 to 30 aromatic ring atoms, which may be substituted by one or more non-aromatic radicals R³; two radicals Ar which are bonded to the same N atom, P atom or B atom may also be bridged to one another by a single bond or a bridge selected from N(R³), C(R³)₂, O or S. The substituent R³ has been described above or is preferably described below.

A cyclic alkyl, alkoxy or thioalkoxy group in the sense of this invention is taken to mean a monocyclic, bicyclic or polycyclic group.

For the purposes of the present invention, a C₁- to C₂₀-alkyl group, in which, in addition, individual H atoms or CH₂ groups may be substituted by the above-mentioned groups, is taken to mean, for example, the radicals methyl, ethyl, n-propyl, i-propyl, cyclopropyl, n-butyl, i-butyl, s-butyl, t-butyl, cyclobutyl, 2-methylbutyl, n-pentyl, s-pentyl, t-pentyl, 2-pentyl, neopentyl, cyclopentyl, n-hexyl, s-hexyl, t-hexyl, 2-hexyl, 3-hexyl, neohexyl, cyclohexyl, 1-methylcyclopentyl, 2-methylpentyl, n-heptyl, 2-heptyl, 3-heptyl, 4-heptyl, cycloheptyl, 1-methylcyclohexyl, n-octyl, 2-ethylhexyl, cyclooctyl, 1-bicyclo[2.2.2]octyl, 2-bicyclo[2.2.2]octyl, 2-(2,6-dimethyl)octyl, 3-(3,7-dimethyl)octyl, adamantyl, trifluoromethyl, pentafluoroethyl, 2,2,2-trifluoroethyl, 1,1-dimethyl-n-hex-1-yl, 1,1-dimethyl-n-hept-1-yl, 1,1-dimethyl-n-oct-1-yl, 1,1-dimethyl-n-dec-1-yl, 1,1-dimethyl-n-dodec-1-yl, 1,1-dimethyl-n-tetradec-1-yl, 1,1-dimethyl-n-hexadec-1-yl, 1,1-dimethyl-n-octadec-1-yl, 1,1-diethyl-n-hex-1-yl, 1,1-diethyl-n-hept-1-yl, 1,1-diethyl-n-oct-1-yl, 1,1-diethyl-n-dec-1-yl, 1,1-diethyl-n-dodec-1-yl, 1,1-diethyl-n-tetradec-1-yl, 1,1-diethyl-n-hexadec-1-yl, 1,1-diethyl-n-octadec-1-yl, 1-(n-propyl)cyclohex-1-yl, 1-(n-butyl)cyclohex-1-yl, 1-(n-hexyl)cyclohex-1-yl, 1-(n-octyl)cyclohex-1-yl and 1-(n-decyl)cyclohex-1-yl.

An alkenyl group is taken to mean, for example, ethenyl, propenyl, butenyl, pentenyl, cyclopentenyl, hexenyl, cyclohexenyl, heptenyl, cycloheptenyl, octenyl, cyclooctenyl or cyclooctadienyl.

An alkynyl group is taken to mean, for example, ethynyl, propynyl, butynyl, pentynyl, hexynyl, heptynyl or octynyl.

A C₁- to C₂₀-alkoxy group is taken to mean, for example, methoxy, trifluoromethoxy, ethoxy, n-propoxy, i-propoxy, n-butoxy, i-butoxy, s-butoxy, t-butoxy or 2-methylbutoxy.

A C₁- to C₂₀-thioalkyl group is taken to mean, for example, S-alkyl groups, for example thiomethyl, 1-thioethyl, 1-thio-i-propyl, 1-thio-n-propyl, 1-thio-butyl, 1-thio-n-butyl or 1-thio-t-butyl.

An aryloxy or heteroaryloxy group having 5 to 40 aromatic ring atoms denotes O-aryl or O-heteroaryl and means that the aryl or heteroaryl group respectively is bonded via an oxygen atom.

An aralkyl or heteroaralkyl group having 5 to 40 aromatic ring atoms means that an alkyl group, as described above, is substituted by an aryl group or heteroaryl group.

A phosphorescent emitter in the sense of the present invention is a compound which exhibits luminescence from an excited state having relatively high spin multiplicity, i.e. a spin state >1, in particular from an excited triplet state. For the purposes of this application, all luminescent complexes containing transition metals or lanthanides are to be regarded as phosphorescent emitters. A more precise definition is given below.

If the composition comprising at least one compound of the formula (1), as described above or preferably described below, and at least one compound of the formula (2), as described above or described below, is employed as matrix material for a phosphorescent emitter, its triplet energy is preferably not significantly less than the triplet energy of the phosphorescent emitter.

The following preferably applies to the triplet level: T₁(emitter)-T₁(matrix)≤0.2 eV, particularly preferably ≤0.15 eV, very particularly preferably ≤0.1 eV. T₁(matrix) here is the triplet level of the matrix material in the emission layer, where this condition applies to each of the two matrix materials, and T₁(emitter) is the triplet level of the phosphorescent emitter. If the emission layer comprises more than two matrix materials, the above-mentioned relationship preferably also applies to each further matrix material.

In a preferred embodiment of the invention, compounds of the formula (1) are selected in which a maximum of 4 variables X, preferably a maximum of 3 variables X, particularly preferably 2 variables X, very particularly preferably 1 variable X, denote/denotes N, and the remaining variables X denote CR.

In a preferred embodiment of the invention, compounds of the formula (1) are selected in which all variables X denote CR, where R in each case, independently on each occurrence, has a meaning indicated above. These compounds are described by the formula (1a)

where R, V and v have a meaning indicated above or preferably indicated below.

The invention accordingly furthermore relates to compositions, as described above, in which the compound of the formula (1) corresponds to a compound of the formula (1a),

where R, V and v have a meaning indicated above or preferably indicated below.

R is selected on each occurrence, identically or differently, from the group consisting of H, D, F, Cl, Br, I, CN, NO₂, N(Ar)₂, N(R²)₂, C(═O)Ar, C(═O)R², P(═O)(Ar)₂, P(Ar)₂, B(Ar)₂, Si(Ar)₃, Si(R²)₃, a straight-chain alkyl, alkoxy or thioalkyl group having 1 to 20 C atoms or a branched or cyclic alkyl, alkoxy or thioalkyl group having 3 to 20 C atoms or an alkenyl group having 2 to 20 C atoms, which may in each case be substituted by one or more radicals R², where one or more non-adjacent CH₂ groups may be replaced by R²C═CR², Si(R²)₂, C═O, C═S, C═NR², P(═O)(R²), SO, SO₂, NR², O, S or CONR² and where one or more H atoms may be replaced by D, F, Cl, Br, I, CN or NO₂, an aromatic or heteroaromatic ring system having 5 to 40 aromatic ring atoms, which may in each case be substituted by one or more radicals R², or an aryloxy or heteroaryloxy group having 5 to 40 aromatic ring atoms, which may be substituted by one or more radicals R², or an aralkyl or heteroaralkyl group having 5 to 40 aromatic ring atoms, which may be substituted by one or more radicals R²; two substituents R which are bonded to the same carbon atom or to adjacent carbon atoms may optionally form a monocyclic or polycyclic, aliphatic, aromatic or heteroaromatic ring system, which may be substituted by one or more radicals R².

In an embodiment of the invention, compounds of the formula (1) or (1a) are preferably selected in which V and v have a meaning given above and 1, 2, 3 or 4 substituents R, preferably 1, 2 or 3 substituents R, particularly preferably 2, 3 or 4 substituents R, very particularly preferably 2 substituents R, do not stand for H, but instead have a meaning as preferably described below.

Preferred substituents R of the compounds of the formula (1) or formula (1a) in the number as described above which do not stand for H, preferably denote a straight-chain alkyl, alkoxy or thioalkyl group having 1 to 20 C atoms or a branched or cyclic alkyl, alkoxy or thioalkyl group having 3 to 20 C atoms, an alkenyl group having 2 to 20 C atoms, which may in each case be substituted by one or more radicals R², an aromatic or heteroaromatic ring system having 5 to 40 aromatic ring atoms, which may in each case be substituted by one or more radicals R², or an aryloxy or heteroaryloxy group having 5 to 40 aromatic ring atoms, which may be substituted by one or more radicals R², or an aralkyl or heteroaralkyl group having 5 to 40 aromatic ring atoms, which may be substituted by one or more radicals R²; two substituents R which are bonded to the same carbon atom or to adjacent carbon atoms may form a monocyclic or polycyclic, aliphatic, aromatic or heteroaromatic ring system, which may be substituted by one or more radicals R².

Particularly preferred substituents R of the compounds of the formula (1) or formula (1a) in the number as described above which do not stand for H preferably denote an aromatic or heteroaromatic ring system having 5 to 40 aromatic ring atoms, which may in each case be substituted by one or more radicals R²; two substituents R which are bonded to the same carbon atom or to adjacent carbon atoms may form a monocyclic or polycyclic, aliphatic, aromatic or heteroaromatic ring system, which may be substituted by one or more radicals R².

Two substituents R in compounds of the formula (1) or (1a) which are in each case adjacent on the same ring of the lactam skeleton or which are adjacent on different rings of the lactam skeleton particularly preferably form the following moieties (S1) to (S12), where # and # represent the respective linking site to the C atoms at which the monocyclic or polycyclic, aliphatic, aromatic or heteroaromatic ring system, which may be substituted by one or more radicals R², forms:

R² in the moieties (S1) to (S12) is preferably H or an aromatic or heteroaromatic ring system having 5 to 40 ring atoms, which may be substituted by R³, preferably H or phenyl.

Very particularly preferred substituents R of the compounds of the formula (1) or formula (1a) in the number as described above which do not stand for H denote an aromatic or heteroaromatic ring system having 5 to 40 ring atoms, which may be substituted by one or more radicals R³, or are preferably selected from ring systems Ar-1 to Ar-22,

where Y³ on each occurrence, identically or differently, denotes O, NR^(#), S or C(R*)₂, where the radical R^(#) that is bonded to N is not equal to H and R³ has the meaning given above or a preferred meaning below and the dashed bond represents the bond to the C atom which carries the respective substituent R.

The radical R^(#) is on each occurrence, identically or differently, H, D, F, Cl, Br, I, CN, NO₂, N(Ar)₂, N(R²)₂, C(═O)Ar, C(═O)R², P(═O)(Ar)₂, P(Ar)₂, B(Ar)₂, Si(Ar)₃, Si(R²)₃, a straight-chain alkyl, alkoxy or thioalkyl group having 1 to 20 C atoms or a branched or cyclic alkyl, alkoxy or thioalkyl group having 3 to 20 C atoms or an alkenyl group having 2 to 20 C atoms, which may in each case be substituted by one or more radicals R², where one or more non-adjacent CH₂ groups may be replaced by R²C═CR², Si(R²)₂, C═O, C═S, C═NR², P(═O)(R²), SO, SO₂, NR², O, S or CONR² and where one or more H atoms may be replaced by D, F, Cl, Br, I, CN or NO₂, an aromatic or heteroaromatic ring system having 5 to 40 aromatic ring atoms, which may in each case be substituted by one or more radicals R², or an aryloxy or heteroaryloxy group having 5 to 40 aromatic ring atoms, which may be substituted by one or more radicals R², or an aralkyl or heteroaralkyl group having 5 to 40 aromatic ring atoms, which may be substituted by one or more radicals R²; two substituents R^(#) which are bonded to the same carbon atom or to adjacent carbon atoms may optionally form a monocyclic or polycyclic, aliphatic, aromatic or heteroaromatic ring system, which may be substituted by one or more radicals R².

Y³ is preferably O, S or C(CH₃)₂. Y³ is particularly preferably O:

The substituent R³ in structures Ar-1 to Ar-22 is selected on each occurrence, identically or differently, from the group consisting of H, D, F, CN, an aliphatic hydrocarbon radical having 1 to 20 C atoms or an aromatic or heteroaromatic ring system having 6 to 30 aromatic ring atoms, in which one or more H atoms may be replaced by D, F, Cl, Br, I or CN and which may be substituted by one or more alkyl groups, each having 1 to 4 carbon atoms; two or more adjacent substituents R³ may form a mono- or polycyclic, aliphatic ring system with one another. The substituent R³ in structures Ar-1 to Ar-22 is preferably selected on each occurrence, identically or differently, from the group consisting of H, F, CN, an aliphatic hydrocarbon radical having 1 to 10 C atoms or an aromatic or heteroaromatic ring system having 5 to 30 aromatic ring atoms. The substituent R³ in structures Ar-1 to Ar-22 is preferably selected on each occurrence, identically or differently, from the group consisting of H or an aromatic or heteroaromatic ring system having 5 to 30 aromatic ring atoms, as described above, but preferably dibenzofuran, dibenzothiophene, 9-phenylcarbazole or spirobifluorene.

Particularly preferably 1, 2 or 3 substituents R, very particularly preferably 2 substituents R, denote Ar-1 to Ar-7, where R³ as a meaning given or preferably given above.

In compounds of the formula (1) or (1a) or preferably described compounds of the formula (1) or (1a), v is preferably 0, corresponding to the formula (1 b),

where R, independently on each occurrence, has a meaning indicated or indicated as preferred above.

In compounds of the formula (1) or (1a) or preferably described compounds of the formula (1) or (1a), v is preferably 1 and V stands for a single bond, corresponding to the formula (1c),

where R, independently on each occurrence, has a meaning indicated or indicated as preferred above.

In compounds of the formula (1) or (1a) or preferably described compounds of the formula (1) or (1a), v is preferably 1, V stands for a single bond and two substituents R stand for a moiety of the formula (S1), corresponding to the formula (1d),

where R and R², independently on each occurrence, have a meaning indicated above or as preferably indicated.

In compounds of the formula (1) or (1a) or preferably described compounds of the formula (1) or (1a), v is preferably 1 and V stands for C(R⁰)₂, O or S, corresponding to the formula (1e),

where R, independently on each occurrence, has a meaning indicated or indicated as preferred above. V is particularly preferably C(R⁰)₂, where R⁰ in each case, independently of one another, has a meaning given above.

Particularly preferred compounds of the formula (1b) are compounds of the formula (1f),

where R, independently on each occurrence, has a meaning indicated or indicated as preferred above.

Particularly preferred compounds of the formula (1c) are compounds of formula (1g),

where R, independently on each occurrence, has a meaning indicated or indicated as preferred above.

The compounds of the formulae (1c) and (1g), as described above, or with preferred substituents R, as described above, are very particularly preferably selected for the composition according to the invention.

Particularly preferred compounds of the formula (1d) are compounds of the formula (1g),

where R, independently on each occurrence, has a meaning indicated or indicated as preferred above.

Particularly preferred compounds of the formula (1e) are compounds of the formula (1i),

where R, independently on each occurrence, has a meaning indicated or indicated as preferred above.

Examples of suitable compounds of the formula (1), (1a), (1b), (1c), (1d), (1e), (1f), (1g), (1h) or (1i) which are selected in accordance with the invention are the structures given below in Table 1.

TABLE 1

L1

L2

L3

L4

L5

L6

L7

L8

L9

L10

L11

L12

L13

L14

L15

L16

L17

L18

L19

L20

L21

L22

L32

L34

L30

L23

L24

L25

L26

L27

L28

L29

L33

Particularly suitable compounds of the formula (1), (1a), (1b), (1c), (1d), (1e), (1f), (1g), (1h) or (1i) which are selected in accordance with the invention are compounds L1 to L34 from Table 2, very particularly preferably compounds L1 to L16.

TABLE 2

L1

L2

L3

L4

L5

L6

L7

L8

L9

L10

L11

L12

L13

L14

L15

L16

L17

L18

L19

L20

L21

L22

L23

L24

L25

L26

L27

L28

L29

L30

L31

L32

L33

L34

The preparation of the compounds of the formula (1) or the preferred compounds of the formulae (1a) to (1i) and compounds L1 to L34 is known to the person skilled in the art. The compounds can be prepared by synthesis steps known to the person skilled in the art, such as, for example, halogenation, preferably bromination, and a subsequent organometallic coupling reaction, for example Suzuki coupling, Heck coupling or Hartwig-Buchwald coupling. The preparation of the compounds of the formula (1) or the preferred compounds of the formulae (1a) to (1i) and compounds L1 to L34 is known, in particular, from WO 2011/137951, pages 42 to 46 and the synthesis examples on pages 48 to 64, from WO 2013/064206 and the synthesis examples on pages 44 to 67, or from WO 2014/094964, pages 54-67.

In an embodiment of the invention, compounds of the formula (2), as described above, are selected which are used in the composition with compounds of the formulae (1), (1a), (1b), (1c), (1d), (1e), (1f), (1g), (1h) and (1i), as described or preferably described above, or with compounds L1 to L34.

The symbol X² in compounds of the formula (2) preferably stands twice for N, particularly preferably once for N, and the remaining groups X² then stand for CR¹, where R¹ in each case, independently of one another, as a meaning indicated above or preferably indicated below.

X² in compounds of the formula (2) is very particularly preferably CR¹, where R¹, independently on each occurrence, has a meaning indicated above or below.

Compounds of the formula (2) in which X² on each occurrence, identically or differently, denotes CR¹ are represented by the formula (2a),

where R¹, Ar₁ and Ar₂ have a meaning given above or a preferred meaning described below and q and t in each case, independently of one another, denote 0, 1, 2, 3 or 4 and r and s in each case, independently of one another, denote 0, 1, 2 or 3.

In compounds of the formula (2a), H is excluded from the definition of the substituents R¹. This exclusion applies correspondingly to all formulae below in which q, t, s and r occur.

The invention accordingly furthermore relates to a composition, as described above, where the compound of the formula (2) corresponds to the compound of the formula (2a).

In a preferred embodiment of the compounds of the formula (2) or (2a), the two carbazoles are linked to one another in position 3 in each case. This embodiment is represented by the compounds of the formula (2b),

where R¹, Ar₁ and Ar₂ have a meaning given above or a preferred meaning described below and q and t in each case, independently of one another, denote 0, 1, 2, 3 or 4 and r and s in each case, independently of one another, denote 0, 1, 2 or 3.

The invention accordingly furthermore relates to a composition, as described above, where the compound of the formula (2) corresponds to the compound of the formula (2b).

Z is preferably C(R⁰)₂, O or S. R⁰ in Z is preferably methyl, ethyl or n-butyl, particularly preferably methyl.

In compounds of the formula (2), (2a) or (2b), Z is particularly preferably C(R⁰)₂.

In compounds of the formula (2), (2a) or (2b), as described or preferably described above, n is preferably 0. This embodiment is represented by the compounds of the formula (2c),

where R¹, Ar₁ and Ar₂ have a meaning given above or a preferred meaning described below and q and t in each case, independently of one another, denote 0, 1, 2, 3 or 4 and r and s in each case, independently of one another, denote 0, 1, 2 or 3.

In compounds of the formula (2), (2a), (2b) or (2c), q is preferably 0, 1 or 2, where R¹ has a meaning indicated above or a meaning indicated below. q is particularly preferably 0 or 1. q is very particularly preferably 0.

If q is greater than 0 in compounds of the formula (2), (2a), (2b) or (2c), the substituent R¹ is preferably selected on each occurrence, identically or differently, from the group consisting of D, F, an alkyl group having 1 to 40 C atoms or an aromatic or heteroaromatic ring system having 5 to 40 aromatic ring atoms, which may be substituted by one or more radicals R². The aromatic or heteroaromatic ring system having 5 to 40 aromatic ring atoms in this R¹ is preferably derived from benzene, dibenzofuran, dibenzothiophene, 9-phenylcarbazole, biphenyl or terphenyl, which may be substituted by one or more radicals R². The preferred position of the substituent(s) [R¹]q is position 1, 2, 3 or 4 or a combination of positions 1 and 4 and 1 and 3, particularly preferably 1 and 3, 2 or 3, very particularly preferably 3, where R¹ has one of the preferred meanings indicated above and q is greater than 0. Particularly preferred substituents R¹ in [R¹]q are phenyl and biphenyl.

In compounds of the formula (2), (2a), (2b) or (2c), r is preferably 0, 1 or 2, where R¹ has a meaning indicated above or a meaning indicated below. r is particularly preferably 0 or 1, very particularly preferably 0.

If r is greater than 0 in compounds of the formula (2), (2a), (2b) or (2c), the substituent R¹ is preferably selected on each occurrence, identically or differently, from the group consisting of D, F, an alkyl group having 1 to 40 C atoms or an aromatic or heteroaromatic ring system having 5 to 40 aromatic ring atoms, which may be substituted by one or more radicals R². The aromatic or heteroaromatic ring system having 5 to 40 aromatic ring atoms in this R¹ is preferably derived from benzene, dibenzofuran, dibenzothiophene, 9-phenylcarbazole, biphenyl and terphenyl, which may be substituted by one or more radicals R². The preferred position of the substituent(s) [R¹]r is position 1 or 2, particularly preferably 1, where R¹ has one of the preferred meanings indicated above and r is greater than 0. Particularly preferred substituents R¹ in [R¹]r are phenyl, 9-phenylcarbazole and 9H-carbazol-9-yl.

In compounds of the formula (2), (2a), (2b) or (2c), s is preferably 0, 1 or 2, where R¹ has a meaning indicated above for a meaning indicated below. s is particularly preferably 0 or 1, very particularly preferably 0.

If s is greater than 0 in compounds of the formula (2), (2a), (2b) or (2c), the substituent R¹ is preferably selected on each occurrence, identically or differently, from the group consisting of D, F, an alkyl group having 1 to 40 C atoms or an aromatic or heteroaromatic ring system having 5 to 40 aromatic ring atoms, which may be substituted by one or more radicals R². The aromatic or heteroaromatic ring system having 5 to 40 aromatic ring atoms in this R¹ is preferably derived from benzene, dibenzofuran, dibenzothiophene, 9-phenylcarbazole, biphenyl or terphenyl, which may be substituted by one or more radicals R². The preferred position of the substituent(s) [R¹]s is position 1 or 2, particularly preferably 1, where R¹ has one of the preferred meanings indicated above and s is greater than 0. Particularly preferred substituents R¹ in [R¹]r are phenyl, 9-phenylcarbazole and 9H-carbazol-9-yl.

In compounds of the formula (2), (2a), (2b) or (2c), t is preferably 0, 1 or 2, where R¹ has a meaning indicated above or a meaning indicated below. t is particularly preferably 0 or 1. t is very particularly preferably 0.

If t is greater than 0 in compounds of the formula (2), (2a), (2b) or (2c), the substituent R¹ is preferably selected on each occurrence, identically or differently, from the group consisting of D, F, an alkyl group having 1 to 40 C atoms or an aromatic or heteroaromatic ring system having 5 to 40 aromatic ring atoms, which may be substituted by one or more radicals R². The aromatic or heteroaromatic ring system having 5 to 40 aromatic ring atoms in this R¹ is preferably derived from benzene, dibenzofuran, dibenzothiophene, 9-phenylcarbazole, biphenyl or terphenyl, which may be substituted by one or more radicals R². The preferred position of the substituent(s) [R¹]q is position 1, 2, 3 or 4 or a combination of positions 1 and 4, 1 and 3, 1 and 2 and 3 and 4, particularly preferably 1 and 3, 2 or 3, very particularly preferably 2 or 3, where R¹ has one of the preferred meanings indicated above and t is greater than 0. Particularly preferred substituents R¹ in [R¹]t are phenyl, biphenyl and terphenyl.

The substituent R² is preferably selected on each occurrence, identically or differently, from the group consisting of D, F, Cl, Br, I, CN, NO₂, N(Ar)₂, NH₂, N(R³)₂, C(═O)Ar, C(═O)H, C(═O)R³, P(═O)(Ar)₂, a straight-chain alkyl, alkoxy or thioalkyl group having 1 to 40 C atoms or a branched or cyclic alkyl, alkoxy or thioalkyl group having 3 to 40 C atoms or an alkenyl or alkynyl group having 2 to 40 C atoms, which may in each case be substituted by one or more radicals R³, or is an aromatic or heteroaromatic ring system having 5 to 60 aromatic ring atoms, which may in each case be substituted by one or more radicals R³, or is an aryloxy or heteroaryloxy group having 5 to 60 aromatic ring atoms, which may be substituted by one or more radicals R³. The substituent R² is particularly preferably on its occurrence an aromatic or heteroaromatic ring system, as described above, preferably selected from the group carbazole, 9-phenylcarbazole, dibenzofuran, dibenzothiophene, fluorene, terphenyl or spirobifluorene, very particularly preferably derived from a dibenzofuran.

In the case of the substitution of one of the substituents R², as described above, by a substituent R³, the meanings of R³ as described above or preferably described apply.

In compounds of the formula (2), (2a), (2b) or (2c), as described above, Ar₁ and Ar₂ are in each case, independently of one another, an aromatic ring system having 6 to 40 aromatic ring atoms or a heteroaromatic ring system having 10 to 40 aromatic ring atoms, which may be substituted by one or more radicals R³. Due to the definition indicated for the radicals R¹ and R³, the composition according to the invention differs from the composition of the emitting layer in the examples of WO 2013/064206 and WO 2014/094964.

In the case of the heteroaromatic ring systems having 10 to 40 C atoms, which may be substituted by one or more of the substituents R³, electron-rich ring systems are particularly preferred, where the ring system which is optionally substituted by R³ preferably contains in total only one N atom or the ring system which is optionally substituted by R³ contains in total one or more O and/or S atoms.

In compounds of the formula (2), (2a), (2b) or (2c) or preferably described compounds of the formula (2), (2a), (2b) or (2c), Ar₁ and Ar₂ are preferably selected from the aromatic or heteroaromatic ring systems Ar-1 to Ar-22, as described above, where the comments regarding the groups R^(#), Y³ and R³ also apply, preferably with the condition that a heteroaromatic ring system represented by Ar-12, Ar-13, Ar-14, Ar-15, Ar-20 and Ar-21 which is optionally substituted by R³ contains in total only one N atom.

In a preferred embodiment of the invention, compounds of the formula (2), (2a), (2b) or (2c) are selected in which one of the substituents Ar₁ and Ar₂ denotes an aromatic ring system having 6 to 40 aromatic ring atoms or a heteroaromatic ring system having 10 to 40 aromatic ring atoms, which may be substituted by one or more radicals R³, and the other substituent denotes an aromatic ring system having 6 to 40 aromatic ring atoms, which may be substituted by one or more radicals R³.

The invention accordingly furthermore relates to a composition, as described above or as preferably described, where one of the substituents Ar₁ and Ar₂ in compounds of the formula (2) or (2a) or (2b) or (2c) denotes an aromatic ring system having 6 to 40 aromatic ring atoms or a heteroaromatic ring system having 10 to 40 aromatic ring atoms, which may be substituted by one or more radicals R³, and the other substituent denotes an aromatic ring system having 6 to 40 aromatic ring atoms, which may be substituted by one or more radicals R³.

In this embodiment, it is preferred if one substituent Ar₁ or Ar₂ corresponds to one of structures Ar-1 to Ar-22, as described above or as preferably described, and the other substituent corresponds to one of structures Ar-1 to Ar-11 or Ar-16 to Ar-19 or Ar-22, preferably with the condition that a heteroaromatic ring system represented by Ar-12, Ar-13, Ar-14, Ar-15, Ar₂₀ and Ar-21 which is optionally substituted by R³ contains in total only one N atom.

In a particularly preferred embodiment of the invention, compounds of the formula (2), (2a), (2b) or (2c) are selected in which the substituents Ar₁ and Ar₂ in each case, independently of one another, denote an aromatic ring system having 6 to 40 aromatic ring atoms, which may be substituted by one or more radicals R³.

The substituents R³, when present in this embodiment, are preferably aromatic and do not contain a heteroatom if Ar₁ and Ar₂ denote an aromatic ring system having 6 to 40 ring atoms.

The invention accordingly furthermore relates to a composition, as described above or as preferably described, where the substituents Ar₁ and Ar₂ in compounds of the formula (2) or (2a) or (2b) or (2c) in each case, independently of one another, denote an aromatic ring system having 6 to 40 aromatic ring atoms, which may be substituted by one or more radicals R³.

In this embodiment, it is preferred if both substituents Ar₁ and Ar₂ in each case, independently of one another, correspond to one of structures Ar-1 to Ar-11 or Ar-16 to Ar-19 or Ar-22, as described above or as preferably described, preferably with the condition that the substituent R³ in an aromatic ring system which is optionally substituted by R³ is selected so that it does not contain a heteroatom.

Examples of suitable compounds of the formula (2), (2a), (2b) or (2c) which are selected in accordance with the invention are the structures shown below in Table 3.

TABLE 3 Structure CAS number

CAS-1454567-05-5

CAS-1352040-89-1

CAS-1336889-25-8

CAS-1800544-05-1

CAS-1800544-08-4

CAS-1800544-08-4

CAS-1800544-09-5

CAS-1800544-10-8

CAS-1800544-11-9

CAS-1800544-04-0

CAS-1842320-52-8

CAS-1842320-53-9

CAS-1842320-54-0

CAS-1842320-55-1

CAS-1842320-56-2

CAS-1842320-57-3

CAS-1410876-33-3

CAS-1842320-58-4

CAS-1410876-47-9

CAS-1842320-59-5

CAS-1848256-38-1

CAS-1865661-14-8

CAS-1870867-25-6

CAS-1884707-32-7

CAS-1889262-88-7

CAS-2018307-89-4

CAS-1454655-29-8

CAS-1454655-33-4

CAS-1454660-22-0

CAS-1907663-27-7

CAS-1548581-24-3

CAS-1548581-27-6

CAS-1548581-29-8

CAS-1548581-37-8

CAS-1548581-40-3

CAS-1943719-62-7

CAS-1548581-42-5

CAS-1942079-50-6

CAS-1548581-44-7

CAS-1942079-51-7

CAS-1943719-63-8

CAS-1955476-12-6

CAS-1619966-75-4

CAS-1955476-13-7

CAS-1955476-15-9

CAS-1955476-28-4

CAS-1955476-30-8

CAS-1955476-32-0

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CAS-2018307-37-2

CAS-2018307-38-3

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CAS-2018307-78-1

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CAS-2085318-64-3

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CAS-1812208-18-6

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CAS-1340669-19-3

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CAS-1340669-33-1

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CAS-1415422-76-2

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CAS-1422451-46-4

CAS-1890157-43-3

CAS-1422451-48-6

CAS-1890157-64-8

CAS-1445952-53-3

CAS-1445952-58-8

CAS-1450933-86-4

CAS-1894194-07-0

CAS-1894194-09-2

CAS-1894194-08-1

CAS-1919031-93-8

CAS-1919031-92-7

CAS-1919031-95-0

CAS-1919031-94-9

CAS-1919031-97-2

CAS-1919031-96-1

CAS-1919031-99-4

CAS-1919031-98-3

CAS-1598389-98-0

CAS-1919032-02-2

CAS-1604034-14-1

CAS-1943719-67-2

CAS-1604034-02-7

CAS-1943719-70-7

CAS-1604034-07-2

CAS-1943719-71-8

CAS-1604034-12-9

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CAS-1622931-00-3

CAS-1604034-15-2

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CAS-1643479-51-9

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CAS-1643479-54-2

CAS-1643479-59-7

CAS-1643479-62-2

CAS-1643479-68-8

CAS-1643479-69-9

CAS-1643479-74-6

CAS-1643479-72-4

CAS-2018307-43-0

CAS-1643479-75-7

CAS-2018307-47-4

CAS-2018307-50-9

CAS-2018307-49-6

CAS-1656982-30-7

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CAS-1704071-12-4

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CAS-1799519-35-9

CAS-1799678-37-7

CAS-2073116-97-7

CAS-2048236-10-6

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CAS-1704071-30-6

CAS-1799959-21-9

CAS-1799959-22-0

CAS-1799959-23-1

CAS-1799959-24-2

CAS-1799959-25-3

CAS-1799959-26-4

CAS-1799959-27-5

CAS-1799959-28-6

CAS-1799959-29-7

CAS-1799959-30-0

CAS-1799959-31-1

CAS-1799959-32-2

CAS-1799959-33-3

CAS-1799959-34-4

CAS-1799959-35-5

CAS-1799959-60-6

CAS-1799959-61-7

CAS-1799959-62-8

CAS-1799959-63-9

CAS-1799959-64-0

CAS-1799959-66-2

CAS-1799959-67-3

CAS-1799959-68-4

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Particularly suitable examples of compounds of the formula (2), (2a), (2b) or (2c) which are selected in accordance with the invention are compounds B1 to B14, as described above.

The preparation of the compounds of the formula (2) or the preferred compounds of the formulae (2a), (2b) and (2c) and the compounds from Table 3 is known to the person skilled in the art from the literature. The compounds can be prepared by synthesis steps known to the person skilled in the art, such as, for example, halogenation, preferably bromination, and a subsequent organometallic coupling reaction, for example Suzuki coupling, Heck coupling or Hartwig-Buchwald coupling. Some of the biscarbazoles of the formula (2) are commercially available.

The compounds of the formula (2) or the preferred compounds of the formulae (2a), (2b) and (2c) in which n denotes 0 can be prepared, for example, in accordance with Scheme 1 or Scheme 2.

Scheme 1, for the preparation of asymmetrical biscarbazoles of the formula (2), (2a), (2b) or (2c) in which n denotes 0:

Scheme 2, for the preparation of symmetrical biscarbazoles of the formula (2), (2a), (2b) or (2c) (Ar₁ and Ar₂ are identical and abbreviated to Ar₁ in the scheme) in which n denotes 0:

Scheme 3, for the preparation of biscarbazoles of the formula (2), (2a), (2b) or (2c) in which n denotes 1:

Further details on the syntheses and further literature citations are described in the experimental part.

The above-mentioned host materials of the formulae (1) and (1a) to (1i) and the preferably described embodiments thereof or the compounds from Table 1 and Table 2 can in accordance with the invention be combined as desired with the said host materials of the formulae (2), (2a), (2b) and (2c) and preferably described embodiments thereof or the compounds from Table 3.

Particularly preferred mixtures of the host materials of the formula (1) with the host materials of the formula (2) for the compositions according to the invention are obtained by combination of compounds L1 to L34 from Table 2 with the compounds from Table 3.

Very particularly preferred mixtures of the host materials of the formula (1) with the host materials of the formula (2) are obtained by combination of compounds L1 to L34 from Table 2 in each case with compounds B1 to B14 from Table 3.

Very particularly preferred mixtures M1 to M224 of the host materials of the formula (1) with the host materials of the formula (2) are obtained by combination of compounds L1 to L16 from Table 2 with compounds B1 to B14 from Table 3, as shown below in Table 4.

TABLE 4 M1 L1 B1 M2 L1 B2 (CAS-1454567-05-5) (CAS-1352040-89-1) M3 L1 B3 M4 L1 B4 (CAS-1643479-47-3) (CAS-1643479-49-5) M5 L1 B5 M6 L1 B6 (CAS-1799958-78-3) (CAS-57102-51-9) M7 L1 B7 M8 L1 B8 (CAS-1427160-09-5) M9 L1 B9 M10 L1 B10 (CAS-1643479-72-4) M11 L1 B11 M12 L1 B12 (CAS-1643479-59-7) M13 L1 B13 M14 L1 B14 (CAS-1643479-68-8) (CAS-2086710-73-6) M15 L2 B1 M16 L2 B2 (CAS-1454567-05-5) (CAS-1352040-89-1) M17 L2 B3 M18 L2 B4 (CAS-1643479-47-3) (CAS-1643479-49-5) M19 L2 B5 M20 L2 B6 (CAS-1799958-78-3) (CAS-57102-51-9) M21 L2 B7 M22 L2 B8 (CAS-1427160-09-5) M23 L2 B9 M24 L2 B10 (CAS-1643479-72-4) M25 L2 B11 M26 L2 B12 (CAS-1643479-59-7) M27 L2 B13 M28 L2 B14 (CAS-1643479-68-8) (CAS-2086710-73-6) M29 L3 B1 M30 L3 B2 (CAS-1454567-05-5) (CAS-1352040-89-1) M31 L3 B3 M32 L3 B4 (CAS-1643479-47-3) (CAS-1643479-49-5) M33 L3 B5 M34 L3 B6 (CAS-1799958-78-3) (CAS-57102-51-9) M35 L3 B7 M36 L3 B8 (CAS-1427160-09-5) M37 L3 B9 M38 L3 B10 (CAS-1643479-72-4) M39 L3 B11 M40 L3 B12 (CAS-1643479-59-7) M41 L3 B13 M42 L3 B14 (CAS-1643479-68-8) (CAS-2086710-73-6) M43 L4 B1 M44 L4 B2 (CAS-1454567-05-5) (CAS-1352040-89-1) M45 L4 B3 M46 L4 B4 (CAS-1643479-47-3) (CAS-1643479-49-5) M47 L4 B5 M48 L4 B6 (CAS-1799958-78-3) (CAS-57102-51-9) M49 L4 B7 M50 L4 B8 (CAS-1427160-09-5) M51 L4 B9 M52 L4 B10 (CAS-1643479-72-4) M53 L4 B11 M54 L4 B12 (CAS-1643479-59-7) M55 L4 B13 M56 L4 B14 (CAS-1643479-68-8) (CAS-2086710-73-6) M57 L5 B1 M58 L5 B2 (CAS-1454567-05-5) (CAS-1352040-89-1) M59 L5 B3 M60 L5 B4 (CAS-1643479-47-3) (CAS-1643479-49-5) M61 L5 B5 M62 L5 B6 (CAS-1799958-78-3) (CAS-57102-51-9) M63 L5 B7 M64 L5 B8 (CAS-1427160-09-5) M65 L5 B9 M66 L5 B10 (CAS-1643479-72-4) M67 L5 B11 M68 L5 B12 (CAS-1643479-59-7) M69 L5 B13 M70 L5 B14 (CAS-1643479-68-8) (CAS-2086710-73-6) M71 L6 B1 M72 L6 B2 (CAS-1454567-05-5) (CAS-1352040-89-1) M73 L6 B3 M74 L6 B4 (CAS-1643479-47-3) (CAS-1643479-49-5) M75 L6 B5 M76 L6 B6 (CAS-1799958-78-3) (CAS-57102-51-9) M77 L6 B7 M78 L6 B8 (CAS-1427160-09-5) M79 L6 B9 M80 L6 B10 (CAS-1643479-72-4) M81 L6 B11 M82 L6 B12 (CAS-1643479-59-7) M83 L6 B13 M84 L6 B14 (CAS-1643479-68-8) (CAS-2086710-73-6) M85 L7 B1 M86 L7 B2 (CAS-1454567-05-5) (CAS-1352040-89-1) M87 L7 B3 M88 L7 B4 (CAS-1643479-47-3) (CAS-1643479-49-5) M89 L7 B5 M90 L7 B6 (CAS-1799958-78-3) (CAS-57102-51-9) M91 L7 B7 M92 L7 B8 (CAS-1427160-09-5) M93 L7 B9 M94 L7 B10 (CAS-1643479-72-4) M95 L7 B11 M96 L7 B12 (CAS-1643479-59-7) M97 L7 B13 M98 L7 B14 (CAS-1643479-68-8) (CAS-2086710-73-6) M99 L8 B1 M100 L8 B2 (CAS-1454567-05-5) (CAS-1352040-89-1) M101 L8 B3 M102 L8 B4 (CAS-1643479-47-3) (CAS-1643479-49-5) M103 L8 B5 M104 L8 B6 (CAS-1799958-78-3) (CAS-57102-51-9) M105 L8 B7 M106 L8 B8 (CAS-1427160-09-5) M107 L8 B9 M108 L8 B10 (CAS-1643479-72-4) M109 L8 B11 M110 L8 B12 (CAS-1643479-59-7) M111 L8 B13 M112 L8 B14 (CAS-1643479-68-8) (CAS-2086710-73-6) M113 L9 B1 M114 L9 B2 (CAS-1454567-05-5) (CAS-1352040-89-1) M115 L9 B3 M116 L9 B4 (CAS-1643479-47-3) (CAS-1643479-49-5) M117 L9 B5 M118 L9 B6 (CAS-1799958-78-3) (CAS-57102-51-9) M119 L9 B7 M120 L9 B8 (CAS-1427160-09-5) M121 L9 B9 M122 L9 B10 (CAS-1643479-72-4) M123 L9 B11 M124 L9 B12 (CAS-1643479-59-7) M125 L9 B13 M126 L9 B14 (CAS-1643479-68-8) (CAS-2086710-73-6) M127 L10 B1 M128 L10 B2 (CAS-1454567-05-5) (CAS-1352040-89-1) M129 L10 B3 M130 L10 B4 (CAS-1643479-47-3) (CAS-1643479-49-5) M131 L10 B5 M132 L10 B6 (CAS-1799958-78-3) (CAS-57102-51-9) M133 L10 B7 M134 L10 B8 (CAS-1427160-09-5) M135 L10 B9 M136 L10 B10 (CAS-1643479-72-4) M137 L10 B11 M138 L10 B12 (CAS-1643479-59-7) M139 L10 B13 M140 L10 B14 (CAS-1643479-68-8) (CAS-2086710-73-6) M141 L11 B1 M142 L11 B2 (CAS-1454567-05-5) (CAS-1352040-89-1) M143 L11 B3 M144 L11 B4 (CAS-1643479-47-3) (CAS-1643479-49-5) M145 L11 B5 M146 L11 B6 (CAS-1799958-78-3) (CAS-57102-51-9) M147 L11 B7 M148 L11 B8 (CAS-1427160-09-5) M149 L11 B9 M150 L11 B10 (CAS-1643479-72-4) M151 L11 B11 M152 L11 B12 (CAS-1643479-59-7) M153 L11 B13 M154 L11 B14 (CAS-1643479-68-8) (CAS-2086710-73-6) M155 L12 B1 M156 L12 B2 (CAS-1454567-05-5) (CAS-1352040-89-1) M157 L12 B3 M158 L12 B4 (CAS-1643479-47-3) (CAS-1643479-49-5) M159 L12 B5 M160 L12 B6 (CAS-1799958-78-3) (CAS-57102-51-9) M161 L12 B7 M162 L12 B8 (CAS-1427160-09-5) M163 L12 B9 M164 L12 B10 (CAS-1643479-72-4) M165 L12 B11 M166 L12 B12 (CAS-1643479-59-7) M167 L12 B13 M168 L12 B14 (CAS-1643479-68-8) (CAS-2086710-73-6) M169 L13 B1 M170 L13 B2 (CAS-1454567-05-5) (CAS-1352040-89-1) M171 L13 B3 M172 L13 B4 (CAS-1643479-47-3) (CAS-1643479-49-5) M173 L13 B5 M174 L13 B6 (CAS-1799958-78-3) (CAS-57102-51-9) M175 L13 B7 M176 L13 B8 (CAS-1427160-09-5) M177 L13 B9 M178 L13 B10 (CAS-1643479-72-4) M179 L13 B11 M180 L13 B12 (CAS-1643479-59-7) M181 L13 B13 M182 L13 B14 (CAS-1643479-68-8) (CAS-2086710-73-6) M183 L14 B1 M184 L14 B2 (CAS-1454567-05-5) (CAS-1352040-89-1) M185 L14 B3 M186 L14 B4 (CAS-1643479-47-3) (CAS-1643479-49-5) M187 L14 B5 M188 L14 B6 (CAS-1799958-78-3) (CAS-57102-51-9) M189 L14 B7 M190 L14 B8 (CAS-1427160-09-5) M191 L14 B9 M192 L14 B10 (CAS-1643479-72-4) M193 L14 B11 M194 L14 B12 (CAS-1643479-59-7) M195 L14 B13 M196 L14 B14 (CAS-1643479-68-8) (CAS-2086710-73-6) M197 L15 B1 M198 L15 B2 (CAS-1454567-05-5) (CAS-1352040-89-1) M199 L15 B3 M200 L15 B4 (CAS-1643479-47-3) (CAS-1643479-49-5) M201 L15 B5 M202 L15 B6 (CAS-1799958-78-3) (CAS-57102-51-9) M203 L15 B7 M204 L15 B8 (CAS-1427160-09-5) M205 L15 B9 M206 L15 B10 (CAS-1643479-72-4) M207 L15 B11 M208 L15 B12 (CAS-1643479-59-7) M209 L15 B13 M210 L15 B14 (CAS-1643479-68-8) (CAS-2086710-73-6) M211 L16 B1 M212 L16 B2 (CAS-1454567-05-5) (CAS-1352040-89-1) M213 L16 B3 M214 L16 B4 (CAS-1643479-47-3) (CAS-1643479-49-5) M215 L16 B5 M216 L16 B6 (CAS-1799958-78-3) (CAS-57102-51-9) M217 L16 B7 M218 L16 B8 (CAS-1427160-09-5) M219 L16 B9 M220 L16 B10 (CAS-1643479-72-4) M221 L16 B11 M222 L16 B12 (CAS-1643479-59-7) M223 L16 B13 M224 L16 B14 (CAS-1643479-68-8) (CAS-2086710-73-6)

The concentration of the electron-transporting host of the formula (1), as described or preferably described above, in the composition according to the invention is in the range from 5% by weight to 90% by weight, preferably in the range from 10% by weight to 85% by weight, more preferably in the range from 20% by weight to 85% by weight, even more preferably in the range from 30% by weight to 80% by weight, very particularly preferably in the range from 20% by weight to 60% by weight and most preferably in the range from 30% by weight to 50% by weight, based on the entire composition.

The concentration of the hole-transporting host of the formula (2), as described above or as preferably described, in the composition is in the range from 10% by weight to 95% by weight, preferably in the range from 15% by weight to 90% by weight, more preferably in the range from 15% by weight to 80% by weight, even more preferably in the range from 20% by weight to 70% by weight, very particularly preferably in the range from 40% by weight to 80% by weight and most preferably in the range from 50% by weight to 70% by weight, based on the entire composition.

In a further preferred embodiment, the composition according to the invention may also comprise further compounds, in particular organic functional materials, besides at least one compound of the formula (1), as described above or as preferably described, as electron-transporting host or electron-transporting matrix material, and at least one compound of the formula (2), as described above or as preferably described, as hole-transporting host or as hole-transporting matrix material. The composition in this embodiment preferably forms an organic layer in an electronic device, as described below.

The present invention therefore also relates to a composition which, besides the above-mentioned materials, also comprises at least one further compound selected from the group consisting of hole-injection materials, hole-transport materials, hole-blocking materials, wide bandgap materials, fluorescent emitters, phosphorescent emitters, host materials, electron-blocking materials, electron-transport materials and electron-injection materials, n-dopants and p-dopants. The person skilled in the art is presented with absolutely no difficulties in selecting these from a multiplicity of materials known to him.

n-Dopants herein are taken to mean reducing agents, i.e. electron donors. Preferred examples of n-dopants are W(hpp)₄ and other electron-rich metal complexes in accordance with WO 2005/086251 A2, P═N compounds (for example WO 2012/175535 A1, WO 2012/175219 A1), naphthylenecarbodiimides (for example WO 2012/168358 A1), fluorenes (for example WO 2012/031735 A1), free radicals and diradicals (for example EP 1837926 A1, WO 2007/107306 A1), pyridines (for example EP 2452946 A1, EP 2463927 A1), N-heterocyclic compounds (for example WO 2009/000237 A1) and acridines as well as phenazines (for example US 2007/145355 A1).

p-Dopants herein are taken to mean oxidants, i.e. electron acceptors. Preferred examples of p-dopants are F4-TCNQ, F6-TNAP, NDP-2 (Novaled), NDP-9 (Novaled), quinones (for example EP 1538684 A1, WO 2006/081780 A1, WO 2009/003455 A1, WO 2010/097433 A1), radialenes (for example EP 1988587 A1, US 2010/102709 A1, EP 2180029 A1, WO 2011/131185 A1, WO 2011134458 A1, US 2012/223296 A1), S-containing transition-metal complexes (for example WO 2007/134873 A1, WO 2008/061517 A2, WO 2008/061518 A2, DE 102008051737 A1, WO 2009/089821 A1, US 2010/096600 A1), bisimidazoles (for example WO 2008/138580 A1), phthalocyanines (for example WO 2008/058525 A2), boratetraazapentalenes (for example WO 2007/115540 A1) fullerenes (for example DE 102010046040 A1) and main-group halides (for example WO 2008/128519 A2).

Wide bandgap material herein is taken to mean a material in the sense of the disclosure of U.S. Pat. No. 7,294,849 which is characterised by a bandgap of at least 3.5 eV, where bandgap is taken to mean the separation between the HOMO and LUMO energy of a material.

The composition according to the invention comprising a bipolar host and an electron-transporting host preferably additionally comprises at least one light-emitting compound or an emitter, where phosphorescent emitters are particularly preferred.

The term phosphorescent emitters typically encompasses compounds in which the light emission takes place through a spin-forbidden transition from an excited state having relatively high spin multiplicity, i.e. a spin state >1, for example through a transition from a triplet state or a state having an even higher spin quantum number, for example a quintet state. This is preferably taken to mean a transition from a triplet state.

Suitable phosphorescent emitters (=triplet emitters) are, in particular, compounds which emit light, preferably in the visible region, on suitable excitation and in addition contain at least one atom having an atomic number greater than 20, preferably greater than 38 and less than 84, particularly preferably greater than 56 and less than 80, in particular a metal having this atomic number. The phosphorescent emitters used are preferably compounds which contain copper, molybdenum, tungsten, rhenium, ruthenium, osmium, rhodium, iridium, palladium, platinum, silver, gold or europium, in particular compounds which contain iridium or platinum. For the purposes of the present invention, all luminescent compounds which contain the above-mentioned metals are regarded as phosphorescent emitters.

In general, suitable phosphorescent complexes are all those as are used in accordance with the prior art for phosphorescent OLEDs and as are known to the person skilled in the art in the area of organic electroluminescent devices.

Examples of the emitters described are revealed by the applications WO 2016/015815, WO 00/70655, WO 2001/41512, WO 2002/02714, WO 2002/15645, EP 1191613, EP 1191612, EP 1191614, WO 05/033244, WO 05/019373, US 2005/0258742, WO 2009/146770, WO 2010/015307, WO 2010/031485, WO 2010/054731, WO 2010/054728, WO 2010/086089, WO 2010/099852, WO 2010/102709, WO 2011/032626, WO 2011/066898, WO 2011/157339, WO 2012/007086, WO 2014/008982, WO 2014/023377, WO 2014/094961, WO 2014/094960, WO 2015/036074, WO 2015/104045, WO 2015/117718, WO 2016/015815, WO 2016/124304, WO 2017/032439, WO 2015/036074, WO 2015/117718 and WO 2016/015815.

Preferred examples of phosphorescent emitters are shown in Table 5 below.

TABLE 5

Preferred examples of phosphorescent polypodal emitters are shown in Table 6 below.

TABLE 6 CAS-1269508-30-6 CAS-1989601-68-4 CAS-1989602-19-8 CAS-1989602-70-1 CAS-1215692-34-4 CAS-1989601-69-5 CAS-1989602-20-1 CAS-1989602-71-2 CAS-1370364-40-1 CAS-1989601-70-8 CAS-1989602-21-2 CAS-1989602-72-3 CAS-1370364-42-3 CAS-1989601-71-9 CAS-1989602-22-3 CAS-1989602-73-4 CAS-1989600-74-9 CAS-1989601-72-0 CAS-1989602-23-4 CAS-1989602-74-5 CAS-1989600-75-0 CAS-1989601-73-1 CAS-1989602-24-5 CAS-1989602-75-6 CAS-1989600-77-2 CAS-1989601-74-2 CAS-1989602-25-6 CAS-1989602-76-7 CAS-1989600-78-3 CAS-1989601-75-3 CAS-1989602-26-7 CAS-1989602-77-8 CAS-1989600-79-4 CAS-1989601-76-4 CAS-1989602-27-8 CAS-1989602-78-9 CAS-1989600-82-9 CAS-1989601-77-5 CAS-1989602-28-9 CAS-1989602-79-0 CAS-1989600-83-0 CAS-1989601-78-6 CAS-1989602-29-0 CAS-1989602-80-3 CAS-1989600-84-1 CAS-1989601-79-7 CAS-1989602-30-3 CAS-1989602-82-5 CAS-1989600-85-2 CAS-1989601-80-0 CAS-1989602-31-4 CAS-1989602-84-7 CAS-1989600-86-3 CAS-1989601-81-1 CAS-1989602-32-5 CAS-1989602-85-8 CAS-1989600-87-4 CAS-1989601-82-2 CAS-1989602-33-6 CAS-1989602-86-9 CAS-1989600-88-5 CAS-1989601-83-3 CAS-1989602-34-7 CAS-1989602-87-0 CAS-1989600-89-6 CAS-1989601-84-4 CAS-1989602-35-8 CAS-1989602-88-1 CAS-1989601-11-7 CAS-1989601-85-5 CAS-1989602-36-9 CAS-1989604-00-3 CAS-1989601-23-1 CAS-1989601-86-6 CAS-1989602-37-0 CAS-1989604-01-4 CAS-1989601-26-4 CAS-1989601-87-7 CAS-1989602-38-1 CAS-1989604-02-5 CAS-1989601-28-6 CAS-1989601-88-8 CAS-1989602-39-2 CAS-1989604-03-6 CAS-1989601-29-7 CAS-1989601-89-9 CAS-1989602-40-5 CAS-1989604-04-7 CAS-1989601-33-3 CAS-1989601-90-2 CAS-1989602-41-6 CAS-1989604-05-8 CAS-1989601-40-2 CAS-1989601-91-3 CAS-1989602-42-7 CAS-1989604-06-9 CAS-1989601-41-3 CAS-1989601-92-4 CAS-1989602-43-8 CAS-1989604-07-0 CAS-1989601-42-4 CAS-1989601-93-5 CAS-1989602-44-9 CAS-1989604-08-1 CAS-1989601-43-5 CAS-1989601-94-6 CAS-1989602-45-0 CAS-1989604-09-2 CAS-1989601-44-6 CAS-1989601-95-7 CAS-1989602-46-1 CAS-1989604-10-5 CAS-1989601-45-7 CAS-1989601-96-8 CAS-1989602-47-2 CAS-1989604-11-6 CAS-1989601-46-8 CAS-1989601-97-9 CAS-1989602-48-3 CAS-1989604-13-8 CAS-1989601-47-9 CAS-1989601-98-0 CAS-1989602-49-4 CAS-1989604-14-9 CAS-1989601-48-0 CAS-1989601-99-1 CAS-1989602-50-7 CAS-1989604-15-0 CAS-1989601-49-1 CAS-1989602-00-7 CAS-1989602-51-8 CAS-1989604-16-1 CAS-1989601-50-4 CAS-1989602-01-8 CAS-1989602-52-9 CAS-1989604-17-2 CAS-1989601-51-5 CAS-1989602-02-9 CAS-1989602-53-0 CAS-1989604-18-3 CAS-1989601-52-6 CAS-1989602-03-0 CAS-1989602-54-1 CAS-1989604-19-4 CAS-1989601-53-7 CAS-1989602-04-1 CAS-1989602-55-2 CAS-1989604-20-7 CAS-1989601-54-8 CAS-1989602-05-2 CAS-1989602-56-3 CAS-1989604-21-8 CAS-1989601-55-9 CAS-1989602-06-3 CAS-1989602-57-4 CAS-1989604-22-9 CAS-1989601-56-0 CAS-1989602-07-4 CAS-1989602-58-5 CAS-1989604-23-0 CAS-1989601-57-1 CAS-1989602-08-5 CAS-1989602-59-6 CAS-1989604-24-1 CAS-1989601-58-2 CAS-1989602-09-6 CAS-1989602-60-9 CAS-1989604-25-2 CAS-1989601-59-3 CAS-1989602-10-9 CAS-1989602-61-0 CAS-1989604-26-3 CAS-1989601-60-6 CAS-1989602-11-0 CAS-1989602-62-1 CAS-1989604-27-4 CAS-1989601-61-7 CAS-1989602-12-1 CAS-1989602-63-2 CAS-1989604-28-5 CAS-1989601-62-8 CAS-1989602-13-2 CAS-1989602-64-3 CAS-1989604-29-6 CAS-1989601-63-9 CAS-1989602-14-3 CAS-1989602-65-4 CAS-1989604-30-9 CAS-1989601-64-0 CAS-1989602-15-4 CAS-1989602-66-5 CAS-1989604-31-0 CAS-1989601-65-1 CAS-1989602-16-5 CAS-1989602-67-6 CAS-1989604-32-1 CAS-1989601-66-2 CAS-1989602-17-6 CAS-1989602-68-7 CAS-1989604-33-2 CAS-1989601-67-3 CAS-1989602-18-7 CAS-1989602-69-8 CAS-1989604-34-3 CAS-1989604-35-4 CAS-1989604-88-7 CAS-1989605-52-8 CAS-1989606-07-6 CAS-1989604-36-5 CAS-1989604-89-8 CAS-1989605-53-9 CAS-1989606-08-7 CAS-1989604-37-6 CAS-1989604-90-1 CAS-1989605-54-0 CAS-1989606-09-8 CAS-1989604-38-7 CAS-1989604-92-3 CAS-1989605-55-1 CAS-1989606-10-1 CAS-1989604-39-8 CAS-1989604-93-4 CAS-1989605-56-2 CAS-1989606-11-2 CAS-1989604-40-1 CAS-1989604-94-5 CAS-1989605-57-3 CAS-1989606-12-3 CAS-1989604-41-2 CAS-1989604-95-6 CAS-1989605-58-4 CAS-1989606-13-4 CAS-1989604-42-3 CAS-1989604-96-7 CAS-1989605-59-5 CAS-1989606-14-5 CAS-1989604-43-4 CAS-1989604-97-8 CAS-1989605-61-9 CAS-1989606-15-6 CAS-1989604-45-6 CAS-1989605-09-5 CAS-1989605-62-0 CAS-1989606-16-7 CAS-1989604-46-7 CAS-1989605-10-8 CAS-1989605-63-1 CAS-1989606-17-8 CAS-1989604-47-8 CAS-1989605-11-9 CAS-1989605-64-2 CAS-1989606-18-9 CAS-1989604-48-9 CAS-1989605-13-1 CAS-1989605-65-3 CAS-1989606-19-0 CAS-1989604-49-0 CAS-1989605-14-2 CAS-1989605-66-4 CAS-1989606-20-3 CAS-1989604-50-3 CAS-1989605-15-3 CAS-1989605-67-5 CAS-1989606-21-4 CAS-1989604-52-5 CAS-1989605-16-4 CAS-1989605-68-6 CAS-1989606-22-5 CAS-1989604-53-6 CAS-1989605-17-5 CAS-1989605-69-7 CAS-1989606-23-6 CAS-1989604-54-7 CAS-1989605-18-6 CAS-1989605-70-0 CAS-1989606-24-7 CAS-1989604-55-8 CAS-1989605-19-7 CAS-1989605-71-1 CAS-1989606-26-9 CAS-1989604-56-9 CAS-1989605-20-0 CAS-1989605-72-2 CAS-1989606-27-0 CAS-1989604-57-0 CAS-1989605-21-1 CAS-1989605-73-3 CAS-1989606-28-1 CAS-1989604-58-1 CAS-1989605-22-2 CAS-1989605-74-4 CAS-1989606-29-2 CAS-1989604-59-2 CAS-1989605-23-3 CAS-1989605-75-5 CAS-1989606-30-5 CAS-1989604-60-5 CAS-1989605-24-4 CAS-1989605-76-6 CAS-1989606-31-6 CAS-1989604-61-6 CAS-1989605-25-5 CAS-1989605-77-7 CAS-1989606-32-7 CAS-1989604-62-7 CAS-1989605-26-6 CAS-1989605-78-8 CAS-1989606-33-8 CAS-1989604-63-8 CAS-1989605-27-7 CAS-1989605-79-9 CAS-1989606-34-9 CAS-1989604-64-9 CAS-1989605-28-8 CAS-1989605-81-3 CAS-1989606-35-0 CAS-1989604-65-0 CAS-1989605-29-9 CAS-1989605-82-4 CAS-1989606-36-1 CAS-1989604-66-1 CAS-1989605-30-2 CAS-1989605-83-5 CAS-1989606-37-2 CAS-1989604-67-2 CAS-1989605-31-3 CAS-1989605-84-6 CAS-1989606-38-3 CAS-1989604-68-3 CAS-1989605-32-4 CAS-1989605-85-7 CAS-1989606-39-4 CAS-1989604-69-4 CAS-1989605-33-5 CAS-1989605-86-8 CAS-1989606-40-7 CAS-1989604-70-7 CAS-1989605-34-6 CAS-1989605-87-9 CAS-1989606-41-8 CAS-1989604-71-8 CAS-1989605-35-7 CAS-1989605-88-0 CAS-1989606-42-9 CAS-1989604-72-9 CAS-1989605-36-8 CAS-1989605-89-1 CAS-1989606-43-0 CAS-1989604-73-0 CAS-1989605-37-9 CAS-1989605-90-4 CAS-1989606-44-1 CAS-1989604-74-1 CAS-1989605-38-0 CAS-1989605-91-5 CAS-1989606-45-2 CAS-1989604-75-2 CAS-1989605-39-1 CAS-1989605-92-6 CAS-1989606-46-3 CAS-1989604-76-3 CAS-1989605-40-4 CAS-1989605-93-7 CAS-1989606-48-5 CAS-1989604-77-4 CAS-1989605-41-5 CAS-1989605-94-8 CAS-1989606-49-6 CAS-1989604-78-5 CAS-1989605-42-6 CAS-1989605-95-9 CAS-1989606-53-2 CAS-1989604-79-6 CAS-1989605-43-7 CAS-1989605-96-0 CAS-1989606-55-4 CAS-1989604-80-9 CAS-1989605-44-8 CAS-1989605-97-1 CAS-1989606-56-5 CAS-1989604-81-0 CAS-1989605-45-9 CAS-1989605-98-2 CAS-1989606-61-2 CAS-1989604-82-1 CAS-1989605-46-0 CAS-1989605-99-3 CAS-1989606-62-3 CAS-1989604-83-2 CAS-1989605-47-1 CAS-1989606-00-9 CAS-1989606-63-4 CAS-1989604-84-3 CAS-1989605-48-2 CAS-1989606-01-0 CAS-1989606-67-8 CAS-1989604-85-4 CAS-1989605-49-3 CAS-1989606-04-3 CAS-1989606-69-0 CAS-1989604-86-5 CAS-1989605-50-6 CAS-1989606-05-4 CAS-1989606-70-3 CAS-1989604-87-6 CAS-1989605-51-7 CAS-1989606-06-5 CAS-1989606-74-7 CAS-1989658-39-0 CAS-2088184-56-7 CAS-2088185-07-1 CAS-2088185-66-2 CAS-1989658-41-4 CAS-2088184-57-8 CAS-2088185-08-2 CAS-2088185-67-3 CAS-1989658-43-6 CAS-2088184-58-9 CAS-2088185-09-3 CAS-2088185-68-4 CAS-1989658-47-0 CAS-2088184-59-0 CAS-2088185-10-6 CAS-2088185-69-5 CAS-1989658-49-2 CAS-2088184-60-3 CAS-2088185-11-7 CAS-2088185-70-8 CAS-2088184-07-8 CAS-2088184-61-4 CAS-2088185-12-8 CAS-2088185-71-9 CAS-2088184-08-9 CAS-2088184-62-5 CAS-2088185-13-9 CAS-2088185-72-0 CAS-2088184-09-0 CAS-2088184-63-6 CAS-2088185-14-0 CAS-2088185-73-1 CAS-2088184-10-3 CAS-2088184-64-7 CAS-2088185-15-1 CAS-2088185-74-2 CAS-2088184-11-4 CAS-2088184-65-8 CAS-2088185-16-2 CAS-2088185-75-3 CAS-2088184-13-6 CAS-2088184-66-9 CAS-2088185-17-3 CAS-2088185-76-4 CAS-2088184-14-7 CAS-2088184-67-0 CAS-2088185-18-4 CAS-2088185-77-5 CAS-2088184-15-8 CAS-2088184-68-1 CAS-2088185-19-5 CAS-2088185-78-6 CAS-2088184-16-9 CAS-2088184-69-2 CAS-2088185-20-8 CAS-2088185-79-7 CAS-2088184-17-0 CAS-2088184-70-5 CAS-2088185-21-9 CAS-2088185-80-0 CAS-2088184-18-1 CAS-2088184-71-6 CAS-2088185-22-0 CAS-2088185-81-1 CAS-2088184-19-2 CAS-2088184-72-7 CAS-2088185-23-1 CAS-2088185-82-2 CAS-2088184-20-5 CAS-2088184-73-8 CAS-2088185-32-2 CAS-2088185-83-3 CAS-2088184-21-6 CAS-2088184-74-9 CAS-2088185-33-3 CAS-2088185-84-4 CAS-2088184-22-7 CAS-2088184-75-0 CAS-2088185-34-4 CAS-2088185-85-5 CAS-2088184-23-8 CAS-2088184-76-1 CAS-2088185-35-5 CAS-2088185-86-6 CAS-2088184-24-9 CAS-2088184-77-2 CAS-2088185-36-6 CAS-2088185-87-7 CAS-2088184-25-0 CAS-2088184-78-3 CAS-2088185-37-7 CAS-2088185-88-8 CAS-2088184-26-1 CAS-2088184-79-4 CAS-2088185-38-8 CAS-2088185-89-9 CAS-2088184-27-2 CAS-2088184-80-7 CAS-2088185-39-9 CAS-2088185-90-2 CAS-2088184-28-3 CAS-2088184-81-8 CAS-2088185-40-2 CAS-2088185-91-3 CAS-2088184-29-4 CAS-2088184-82-9 CAS-2088185-41-3 CAS-2088185-92-4 CAS-2088184-30-7 CAS-2088184-83-0 CAS-2088185-42-4 CAS-2088185-93-5 CAS-2088184-32-9 CAS-2088184-84-1 CAS-2088185-43-5 CAS-2088185-94-6 CAS-2088184-34-1 CAS-2088184-85-2 CAS-2088185-44-6 CAS-2088185-95-7 CAS-2088184-35-2 CAS-2088184-86-3 CAS-2088185-45-7 CAS-2088185-96-8 CAS-2088184-36-3 CAS-2088184-87-4 CAS-2088185-46-8 CAS-2088185-97-9 CAS-2088184-37-4 CAS-2088184-88-5 CAS-2088185-47-9 CAS-2088185-98-0 CAS-2088184-38-5 CAS-2088184-89-6 CAS-2088185-48-0 CAS-2088185-99-1 CAS-2088184-39-6 CAS-2088184-90-9 CAS-2088185-49-1 CAS-2088186-00-7 CAS-2088184-40-9 CAS-2088184-91-0 CAS-2088185-50-4 CAS-2088186-01-8 CAS-2088184-41-0 CAS-2088184-92-1 CAS-2088185-51-5 CAS-2088186-02-9 CAS-2088184-42-1 CAS-2088184-93-2 CAS-2088185-52-6 CAS-2088195-88-2 CAS-2088184-43-2 CAS-2088184-94-3 CAS-2088185-53-7 CAS-2088195-89-3 CAS-2088184-44-3 CAS-2088184-95-4 CAS-2088185-54-8 CAS-2088195-90-6 CAS-2088184-45-4 CAS-2088184-96-5 CAS-2088185-55-9 CAS-2088195-91-7 CAS-2088184-46-5 CAS-2088184-97-6 CAS-2088185-56-0 CAS-861806-70-4 CAS-2088184-47-6 CAS-2088184-98-7 CAS-2088185-57-1 CAS-1269508-30-6 CAS-2088184-48-7 CAS-2088184-99-8 CAS-2088185-58-2 CAS-2088184-49-8 CAS-2088185-00-4 CAS-2088185-59-3 CAS-2088184-50-1 CAS-2088185-01-5 CAS-2088185-60-6 CAS-2088184-51-2 CAS-2088185-02-6 CAS-2088185-61-7 CAS-2088184-52-3 CAS-2088185-03-7 CAS-2088185-62-8 CAS-2088184-53-4 CAS-2088185-04-8 CAS-2088185-63-9 CAS-2088184-54-5 CAS-2088185-05-9 CAS-2088185-64-0 CAS-2088184-55-6 CAS-2088185-06-0 CAS-2088185-65-1

In the composition according to the invention, each mixture M1, M2, M3, M4, M5, M6, M7, M8, M9, M10, M11, M12, M13, M14, M15, M16, M17, M18, M19, M20, M21, M22, M23, M24, M25, M26, M27, M28, M29, M30, M31, M32, M33, M34, M35, M36, M37, M38, M39, M40, M41, M42, M43, M44, M45, M46, M47, M48, M49, M50, M51, M52, M53, M54, M55, M56, M57, M58, M59, M60, M61, M62, M63, M64, M65, M66, M67, M68, M69, M70, M71, M72, M73, M74, M75, M76, M77, M78, M79, M80, M81, M82, M83, M84, M85, M86, M87, M88, M89, M90, M91, M92, M93, M94, M95, M96, M97, M98, M99, M100,

M101, M102, M103, M104, M105, M106, M107, M108, M109, M110, M111, M112, M113, M114, M115, M116, M117, M118, M119, M120, M121, M122, M123, M124, M125, M126, M127, M128, M129, M130, M131, M132, M133, M134, M135, M136. M137, M138, M139, M140, M141, M142, M143, M144, M145, M146, M147, M148, M149, M150, M151, M152, M153, M154, M155, M156, M157, M158, M159, M160, M161, M162, M163, M164, M165, M166, M167, M168, M169, M170, M171, M172, M173, M174, M175, M176, M177, M178, M179, M180, M181, M182, M183, M184, M185, M186, M187, M188, M189, M190, M191, M192, M193, M194, M195, M196, M197, M198, M199, M200,

M201, M202, M203, M204, M205, M206, M207, M208, M209, M210, M211, M212, M213, M214, M215, M216, M217, M218, M219, M220, M221, M222, M223 or M224 is preferably combined with a compound from Table 5 or 6.

The composition according to the invention comprising at least one phosphorescent emitter preferably forms an infrared-, yellow-, orange-, red-, green-, blue- or ultraviolet-emitting layer, particularly preferably a yellow- or green-emitting layer and very particularly preferably a green-emitting layer.

A yellow-emitting layer here is taken to mean a layer whose photoluminescence maximum is in the range from 540 to 570 nm. An orange-emitting layer is taken to mean a layer whose photoluminescence maximum is in the range from 570 to 600 nm. A red-emitting layer is taken to mean a layer whose photoluminescence maximum is in the range from 600 to 750 nm. A green-emitting layer is taken to mean a layer whose photoluminescence maximum is in the range from 490 to 540 nm. A blue-emitting layer is taken to mean a layer whose photoluminescence maximum is in the range from 440 to 490 nm. The photoluminescence of the layer is determined here by measurement of the photoluminescence spectrum of the layer having a layer thickness of 50 nm at room temperature, where the layer comprises the composition according to the invention, i.e. comprises emitter and matrix.

The photoluminescence spectrum of the layer is recorded, for example, using a commercially available photoluminescence spectrometer.

The photoluminescence spectrum of the selected emitter is generally measured in oxygen-free solution, 10−5 molar, where the measurement is carried out at room temperature and any solvent in which the selected emitter dissolves in the said concentration is suitable. Particularly suitable solvents are usually toluene or 2-methyl-THF, but also dichloromethane.

The measurement is carried out using a commercially available photoluminescence spectrometer. The triplet energy T₁ in eV is determined from the photoluminescence spectra of the emitters. Firstly the peak maximum PImax. (in nm) of the photoluminescence spectrum is determined. The peak maximum PImax. (in nm) is then converted into in eV in accordance with: E(T1 in eV)=1240/E(T1 in nm)=1240/PImax. (in nm).

Preferred phosphorescent emitters are accordingly infrared emitters, preferably from Table 5 or 6, whose triplet energy T₁ is preferably ˜1.9 eV to ˜1.0 eV.

Preferred phosphorescent emitters are accordingly red emitters, preferably from Table 5 or 6, whose triplet energy T₁ is preferably ˜2.1 eV to ˜1.9 eV.

Preferred phosphorescent emitters are accordingly yellow emitters, preferably from Table 5 or 6, whose triplet energy T₁ is preferably ˜2.3 eV to ˜2.1 eV.

Preferred phosphorescent emitters are accordingly green emitters, preferably from Table 5 or 6, whose triplet energy T₁ is preferably ˜2.5 eV to ˜2.3 eV.

Preferred phosphorescent emitters are accordingly blue emitters, preferably from Table 5 or 6, whose triplet energy T₁ is preferably ˜3.1 eV to ˜2.5 eV.

Preferred phosphorescent emitters are accordingly ultraviolet Emitter, preferably from Table 5 or 6, whose triplet energy T₁ is preferably ˜4.0 eV to ˜3.1 eV.

Particularly preferred phosphorescent emitters are accordingly green or yellow emitters, preferably from Table 5 or 6, as described above. Very particularly preferred phosphorescent emitters are accordingly green emitters, preferably from Table 5 or 6, whose triplet energy T₁ is preferably ˜2.5 eV to ˜2.3 eV.

Green emitters, preferably from Table 5 or 6, as described above, are very particularly preferably selected for the composition according to the invention or the emitting layer according to the invention.

Preferred fluorescent emitters are selected from the class of the arylamines. An arylamine or aromatic amine in the sense of this invention is taken to mean a compound which contains three substituted or unsubstituted aromatic or heteroaromatic ring systems bonded directly to the nitrogen.

At least one of these aromatic or heteroaromatic ring systems is preferably a condensed ring system, particularly preferably having at least 14 aromatic ring atoms. Preferred examples thereof are aromatic anthracenamines, aromatic anthracenediamines, aromatic pyrenamines, aromatic pyrenediamines, aromatic chrysenamines or aromatic chrysenediamines. An aromatic anthracenamine is taken to mean a compound in which one diarylamino group is bonded directly to an anthracene group, preferably in the 9-position. An aromatic anthracenediamine is taken to mean a compound in which two diarylamino groups are bonded directly to an anthracene group, preferably in the 9,10-position. Aromatic pyrenamines, pyrenediamines, chrysenamines and chrysenediamines are defined analogously thereto, where the diarylamino groups are preferably bonded to the pyrene in the 1 position or in the 1,6 position. Further preferred fluorescent emitters are indenofluorenamines or indenofluorenediamines, for example in accordance with WO 2006/108497 or WO 2006/122630, benzoindenofluorenamines or benzoindenofluorenediamines, for example in accordance with WO 2008/006449, and dibenzoindenofluorenamines or dibenzoindenofluorenediamines, for example in accordance with WO 2007/140847, and the indenofluorene derivatives containing condensed aryl groups which are disclosed in WO 2010/012328.

In a further preferred embodiment of the invention, the composition according to the invention is used as a component of mixed-matrix systems. The mixed-matrix systems preferably comprise three or four different matrix materials, particularly preferably three different matrix materials (i.e. a further matrix component in addition to the composition according to the invention). Particularly suitable matrix materials which can be used in combination with the composition according to invention as matrix components of a mixed-matrix system are selected from wide bandgap materials, electron-transport materials (ETMs) and hole-transport materials (HTMs).

Mixed-matrix systems are preferably employed in phosphorescent organic electroluminescent devices. More precise details on mixed-matrix systems are given, inter alia, in the application WO 2010/108579. Particularly suitable matrix materials which can be employed in combination with the composition according to the invention as matrix components of a mixed-matrix system in phosphorescent or fluorescent organic electroluminescent devices are selected from the preferred matrix materials indicated below for phosphorescent emitters or the preferred matrix materials for fluorescent emitters, depending on what type of emitter is employed. The mixed-matrix system is preferably optimised for an emitter from Table 5 or 6.

Suitable further host materials, preferably for fluorescent emitters, besides the composition according to the invention, as described above, particularly preferably comprising a mixture of materials selected from M1 to M224, are various classes of substance. Preferred further host materials are selected from the classes of the oligoarylenes (for example 2,2′,7,7′-tetraphenylspirobifluorene in accordance with EP 676461 or dinaphthylanthracene), in particular the oligoarylenes containing condensed aromatic groups, the oligoarylenevinylenes (for example DPVBi or spiro-DPVBi in accordance with EP 676461), the polypodal metal complexes (for example in accordance with WO 2004/081017), the hole-conducting compounds (for example in accordance with WO 2004/058911), the electron-conducting compounds, in particular ketones, phosphine oxides, sulfoxides, etc. (for example in accordance with WO 2005/084081 and WO 2005/084082), the atropisomers (for example in accordance with WO 2006/048268), the boronic acid derivatives (for example in accordance with WO 2006/117052) or the benzanthracenes (for example in accordance with WO 2008/145239). Particularly preferred matrix materials are selected from the classes of the oligoarylenes, contaning naphthalene, anthracene, benzanthracene and/or pyrene or atropisomers of these compounds, the oligoarylenevinylenes, the ketones, the phosphine oxides and the sulfoxides. Very particularly preferred matrix materials are selected from the classes of the oligoarylenes, containing anthracene, benzanthracene, benzophenanthrene and/or pyrene or atropisomers of these compounds. An oligoarylene in the sense of this invention is intended to be taken to mean a compound in which at least three aryl or arylene groups are bonded to one another.

Suitable further matrix materials, preferably for phosphorescent emitters, besides the composition according to the invention, as described above, particularly preferably comprising a mixture of materials selected from M1 to M224, are various classes of substance. Preferred further matrix materials are selected from the classes of the aromatic amines, in particular triarylamines, for example in accordance with US 2005/0069729, carbazole derivatives (for example CBP, N,N-biscarbazolylbiphenyl) or compounds in accordance with WO 2005/039246, US 2005/0069729, JP 2004/288381, EP 1205527 or WO 2008/086851, bridged carbazole derivatives, for example in accordance with WO 2011/088877 and WO 2011/128017, indenocarbazole derivatives, for example in accordance with WO 2010/136109 and WO 2011/000455, azacarbazole derivatives, for example in accordance with EP 1617710, EP 1617711, EP 1731584, JP 2005/347160, indolocarbazole derivatives, for example in accordance with WO 2007/063754 or WO 2008/056746, ketones, for example in accordance with WO 2004/093207 or WO 2010/006680, phosphine oxides, sulfoxides and sulfones, for example in accordance with WO 2005/003253, oligophenylenes, bipolar matrix materials, for example in accordance with WO 2007/137725, silanes, for example in accordance with WO 2005/111172, azaboroles or boronic esters, for example in accordance with WO 2006/117052, triazine derivatives, for example in accordance with WO 2010/015306, WO 2007/063754 or WO 2008/056746, zinc complexes, for example in accordance with EP 652273 or WO 2009/062578, aluminium complexes, for example BAIq, diazasilole and tetraazasilole derivatives, for example in accordance with WO 2010/054729, diazaphosphole derivatives, for example in accordance with WO 2010/054730, and aluminium complexes, for example BAlQ.

According to an alternative embodiment of the present invention, the composition comprises no further constituents, i.e. functional materials, besides the constituents of electron-transporting host and hole-transporting host.

The invention accordingly furthermore relates to a composition consisting of a compound of the formula (1), (1a) to (1i) or a compound selected from L1 to L34 and a compound of the formula (2) or (2a) to (2c) or a compound selected from B1 to B14.

The composition according to the invention, as described or preferably described above, is suitable for use in an organic electronic device. An organic electronic device here is taken to mean a device which contains at least one layer which comprises at least one organic compound. However, the device may also contain inorganic materials or also layers which are built up entirely from inorganic materials.

The invention accordingly furthermore relates to the use of a composition, as described or preferably described above, in particular a mixture selected from M1 to M224, in an organic electronic device.

The components or constituents of the compositions can be processed by vapour deposition or from solution. If the compositions are applied from solution, formulations of the composition according to the invention comprising at least one further solvent are necessary. These formulations can be, for example, solutions, dispersions or emulsions. It may be preferred to use mixtures of two or more solvents for this purpose.

The present invention therefore furthermore relates to a formulation comprising a composition according to the invention and at least one solvent.

Suitable and preferred solvents are, for example, toluene, anisole, o-, m- or p-xylene, methyl benzoate, mesitylene, tetralin, veratrol, THF, methyl-THF, THP, chlorobenzene, dioxane, phenoxytoluene, in particular 3-phenoxytoluene, (−)-fenchone, 1,2,3,5-tetramethylbenzene, 1,2,4,5-tetramethylbenzene, 1-methylnaphthalene, 2-methylbenzothiazole, 2-phenoxyethanol, 2-pyrrolidinone, 3-methylanisole, 4-methylanisole, 3,4-dimethylanisole, 3,5-dimethylanisole, acetophenone, α-terpineol, benzothiazole, butyl benzoate, cumene, cyclohexanol, cyclohexanone, cyclohexylbenzene, decalin, dodecylbenzene, ethyl benzoate, indane, methyl benzoate, NMP, p-cymene, phenetol, 1,4-diisopropylbenzene, dibenzyl ether, diethylene glycol butyl methyl ether, triethylene glycol butyl methyl ether, diethylene glycol dibutyl ether, triethylene glycol dimethyl ether, diethylene glycol monobutyl ether, tripropylene glycol dimethyl ether, tetraethylene glycol dimethyl ether, 2-isopropylnaphthalene, pentylbenzene, hexylbenzene, heptylbenzene, octylbenzene, 1,1-bis(3,4-dimethylphenyl)ethane, hexamethylindane or mixtures of these solvents.

The formulation here may also comprise at least one further organic or inorganic compound which is likewise employed in the electronic device, in particular an emitting compound, in particular a phosphorescent emitter, and/or a further matrix material. Suitable emitting compounds and further matrix materials have already been mentioned above.

The present invention also relates to the use of the composition according to the invention in an organic electronic device, preferably in an electron-transporting and/or emitting layer.

The organic electronic devices is preferably selected from organic integrated circuits (OICs), organic field-effect transistors (OFETs), organic thin-film transistors (OTFTs), organic electroluminescent devices, organic solar cells (OSCs), organic optical detectors and organic photoreceptors, where organic electroluminescent devices are particularly preferred.

Very particularly preferred organic electroluminescent devices for use of the composition according to the invention are organic light-emitting transistors (OLETs), organic field-quench devices (OFQDs), organic light-emitting electrochemical cells (OLECs, LECs, LEECs), organic laser diodes (O-lasers) and organic light-emitting diodes (OLEDs), particularly preferably OLECs and OLEDs and most preferably OLEDs.

The composition according to the invention, as described above or as preferably described, is preferably used in an electronic device in a layer having an electron-transporting function. The layer is preferably an electron-injection layer (EIL), an electron-transport layer (ETL), a hole-blocking layer (HBL) and/or an emission layer (EML), particularly preferably eine ETL, EIL and/or EML. The composition according to the invention is particularly preferably employed in an EML in particular as matrix material.

The present invention therefore still furthermore relates to an organic electronic device which is selected, in particular, from one of the electronic devices mentioned above and which preferably contains the summary according to the invention, as described or preferably described above, in an emission layer (EML), in an electron-transport layer (ETL), in an electron-injection layer (EIL) and/or in a hole-blocking layer (HBL), very preferably in an EML, EIL and/or ETL and very particularly preferably in an EML.

In the case of an emitting layer, this is particularly preferably a phosphorescent layer which is characterised in that, in addition to the composition as described or preferably described above, it comprises a phosphorescent emitter, in particular together with an emitter from Table 5 or 6 or a preferred emitter, as described above.

In a particularly preferred embodiment of the present invention, the electronic device is therefore an organic electroluminescent device, very particularly preferably an organic light-emitting diode (OLED), which contains the composition according to the invention, as described or preferably described above, together with a phosphorescent emitter in the emission layer (EML).

The composition according to the invention in accordance with the preferred embodiments and the emitting compound preferably comprises between 99.9 and 1% by vol., further preferably between 99 and 10% by vol., particularly preferably between 98 and 60% by vol., very particularly preferably between 97 and 80% by vol., of matrix material comprising at least one compound of the formula (1) and at least one compound of the formula (2) in accordance with the preferred embodiments, based on the entire composition comprising emitter and matrix materials.

Correspondingly, the composition preferably comprises between 0.1 and 99% by vol., further preferably between 1 and 90% by vol., particularly preferably between 2 and 40% by vol., very particularly preferably between 3 and 20% by vol., of the emitter, based on the entire mixture comprising emitter and matrix material. If the compounds are processed from solution, the corresponding amounts in % by weight are preferably used instead of the above-mentioned amounts in % by vol.

Apart from cathode, anode and the layer comprising the composition according to the invention, an electronic device may also comprise further layers. These are selected, for example, from in each case one or more hole-injection layers, hole-transport layers, hole-blocking layers, emitting layers, electron-transport layers, electron-injection layers, electron-blocking layers, exciton-blocking layers, interlayers, charge-generation layers (IDMC 2003, Taiwan; Session 21 OLED (5), T. Matsumoto, T. Nakada, J. Endo, K. Mori, N. Kawamura, A. Yokoi, J. Kido, Multiphoton Organic EL Device Having Charge Generation Layer) and/or organic or inorganic p/n junctions. However, it should be pointed out that each of these layers does not necessarily have to be present.

The sequence of the layers in an organic electroluminescent device device is preferably the following:

anode/hole-injection layer/hole-transport layer/emitting layer/electron-transport layer/electron-injection layer/cathode.

This sequence of the layers is a preferred sequence.

It should again be pointed out here that not all of the said layers have to be present, and/or that further layers may additionally be present.

An organic electroluminescent device which contains the composition according to the invention according to the invention may comprise a plurality of emitting layers. These emission layers in this case particularly preferably have in total a plurality of emission maxima between 380 nm and 750 nm, resulting overall in white emission, i.e. various emitting compounds which are able to fluoresce or phosphoresce and which emit blue or yellow or orange or red light are used in the emitting layers. Particular preference is given to three-layer systems, i.e. systems having three emitting layers, where the three layers exhibit blue, green and orange or red emission (for the basic structure see, for example, WO 2005/011013). It should be noted that, for the generation of white light, one emitter compound used individually which emits in a broad wavelength range may also be suitable instead of a plurality of emitter compounds emitting in colour.

Suitable charge-transport materials, as can be used in the hole-injection or hole-transport layer or electron-blocking layer or in the electron-transport layer of the organic electroluminescent device according to the invention, are, for example, the compounds disclosed in Y. Shirota et al., Chem. Rev. 2007, 107(4), 953-1010 or other materials as are employed in accordance with the prior art in these layers.

Materials which can be used for the electron-transport layer are all materials as are used in accordance with the prior art as electron-transport materials in the electron-transport layer. Particularly suitable are aluminium complexes, for example Alq₃, zirconium complexes, for example Zrq₄, benzimidazole derivatives, triazine derivatives, pyrimidine derivatives, pyridine derivatives, pyrazine derivatives, quinoxaline derivatives, quinoline derivatives, oxadiazole derivatives, aromatic ketones, lactams, boranes, diazaphosphole derivatives and phosphine oxide derivatives. Furthermore suitable materials are derivatives of the above-mentioned compounds, as disclosed in JP 2000/053957, WO 2003/060956, WO 2004/028217, WO 2004/080975 and WO 2010/072300.

Preferred hole-transport materials are, in particular, materials which can be used in a hole-transport, hole-injection or electron-blocking layer, such as indenofluorenamine derivatives (for example in accordance with WO 06/122630 or WO 06/100896), the amine derivatives disclosed in EP 1661888, hexaazatriphenylene derivatives (for example in accordance with WO 01/049806), amine derivatives containing condensed aromatic rings (for example in accordance with U.S. Pat. No. 5,061,569), the amine derivatives disclosed in WO 95/09147, monobenzoindenofluorenamines (for example in accordance with WO 08/006449), dibenzoindenofluorenamines (for example in accordance with WO 07/140847), spirobifluorenamines (for example in accordance with WO 2012/034627 or the as yet unpublished EP 12000929.5), fluorenamines (for example in accordance with WO 2014/015937, WO 2014/015938 and WO 2014/015935), spirodibenzopyranamines (for example in accordance with WO 2013/083216) and dihydroacridine derivatives (for example in accordance with WO 2012/150001).

The cathode of electronic devices preferably comprises metals having a low work function, metal alloys or multilayered structures comprising various metals, such as, for example, alkaline-earth metals, alkali metals, main-group metals or lanthanoids (for example Ca, Ba, Mg, Al, In, Mg, Yb, Sm, etc.). Also suitable are alloys comprising an alkali metal or alkaline-earth metal and silver, for example an alloy comprising magnesium and silver. In the case of multilayered structures, further metals which have a relatively high work function, such as, for example, Ag or Al, can also be used in addition to the said metals, in which case combinations of the metals, such as, for example, Ca/Ag, Mg/Ag or Ba/Ag, are generally used. It may also be preferred to introduce a thin interlayer of a material having a high dielectric constant between a metallic cathode and the organic semiconductor. Suitable for this purpose are, for example, alkali metal fluorides or alkaline-earth metal fluorides, but also the corresponding oxides or carbonates (for example LiF, Li₂O, BaF₂, MgO, NaF, CsF, Cs₂CO₃, etc.). Furthermore, lithium quinolinate (LiQ) can be used for this purpose. The layer thickness of this layer is preferably between 0.5 and 5 nm.

The anode preferably comprises materials having a high work function. The anode preferably has a work function of greater than 4.5 eV vs. vacuum. Suitable for this purpose are on the one hand metals having a high redox potential, such as, for example, Ag, Pt or Au. On the other hand, metal/metal oxide electrodes (for example Al/Ni/NiO_(x), Al/PtO_(x)) may also be preferred. For some applications, at least one of the electrodes must be transparent or partially transparent in order to facilitate either irradiation of the organic material (organic solar cells) or the coupling-out of light (OLEDs, O-lasers). Preferred anode materials here are conductive mixed metal oxides. Particular preference is given to indium tin oxide (ITO) or indium zinc oxide (IZO). Preference is furthermore given to conductive, doped organic materials, in particular conductive doped polymers. Furthermore, the anode may also consist of a plurality of layers, for example of an inner layer of ITO and an outer layer of a metal oxide, preferably tungsten oxide, molybdenum oxide or vanadium oxide.

During production, the organic electronic device is appropriately (depending on the application) structured, provided with contacts and finally sealed, since the lifetime of the devices according to the invention is shortened in the presence of water and/or air.

In a further preferred embodiment, the organic electronic device which contains the composition according to the invention is characterised in that one or more organic layers comprising the compositions according to the invention are applied by means of a sublimation process, in which the materials are applied by vapour deposition in vacuum sublimation units at an initial pressure of less than 10⁻⁵ mbar, preferably less than 10⁻⁶ mbar. However, it is also possible here for the initial pressure to be even lower, for example less than 10⁻⁷ mbar.

Preference is likewise given to an organic electroluminescent device, characterised in that one or more layers are applied by means of the OVPD (organic vapour phase deposition) process or with the aid of carrier-gas sublimation, in which the materials are applied at a pressure of between 10⁻⁵ mbar and 1 bar. A special case of this process is the OVJP (organic vapour jet printing) process, in which the materials are applied directly through a nozzle and are thus structured (for example M. S. Arnold et al., Appl. Phys. Lett. 2008, 92, 053301).

Preference is furthermore given to an organic electroluminescent device, characterised in that one or more layers are produced from solution, such as, for example, by spin coating, or by means of any desired printing process, such as, for example, screen printing, flexographic printing, nozzle printing or offset printing, but particularly preferably LITI (light induced thermal imaging, thermal transfer printing) or ink-jet printing. Soluble compounds of the components of the composition according to the invention are necessary for this purpose. High solubility can be achieved through suitable substitution of the corresponding compounds. Processing from solution has the advantage that the layer comprising the composition according to the invention can be applied very simply and inexpensively. This technique is suitable, in particular, for the mass production of organic electronic devices.

Also possible are hybrid processes, in which, for example, one or more layers are applied from solution and one or more further layers are applied by vapour deposition.

These processes are generally known to the person skilled in the art and can be applied to organic electroluminescent devices.

The invention therefore furthermore relates to a process for the production of an organic electronic device containing a composition according to the invention, as described or preferably described above, characterised in that at least one organic layer comprising a composition according to the invention is applied by gas-phase deposition, in particular by means of a sublimation process and/or by means of an OVPD (organic vapour phase deposition) process and/or with the aid of carrier-gas sublimation, or from solution, in particular by spin coating or by means of a printing process.

In the case of the production of an organic electronic device by means of gas-phase deposition, there are basically two possibilities for how an organic layer which is intended to comprise the composition according to invention and which may comprise a plurality of different constituents can be applied or vapour-deposited onto any desired substrate. On the one hand, the materials used may each be present in one material source and finally evaporated out of the various material sources (“co-evaporation”). On the other hand, the various materials may be premixed and the mixture may be presented in a single material source, from which it is finally evaporated (“premix evaporation”). This enables the vapour-deposition of a layer having a uniform distribution of the components to be achieved in a simple and rapid manner without precise control of a multiplicity of material sources being necessary.

The invention accordingly furthermore relates to a process, characterised in that the at least one compound of the formula (1), as described above or as preferably described, and the at least one compound of the formula (2), as described above or as preferably described, are deposited from the gas phase successively or simultaneously from at least two material sources, optionally with further materials, as described or preferably described above, and form the organic layer.

In a preferred embodiment of the present invention, the at least one organic layer is applied by means of gas-phase deposition, where the constituents of the composition are premixed and evaporated from a single material source.

The invention accordingly furthermore relates to a process, characterised in that the composition according to the invention, as described or preferably described above, is utilised as material source for the gas-phase deposition and forms the organic layer, optionally with further materials.

The invention furthermore relates to a process for the production of an organic electronic device containing a composition according to the invention, as described or preferably described above, characterised in that the formulation according to the invention, as described above, is used in order to apply the organic layer.

The compositions according to the invention or the devices according to the invention are distinguished by the following surprising advantages over the prior art: The use of the compositions according to the invention in organic electronic devices, in particular in organic electroluminescent devices, and in particular in an OLED or OLEC, leads to significant increases in the lifetime of the devices.

As can be seen in Example 1 indicated below, the use of two electron-transporting hosts (for example a lactam derivative and a triazine-carbazole derivative) with emitter concentrations in the EML of 10% of a green emitter leads to a good voltage and moderate efficiency. However, the lifetime of the components is short (V1 and V2). It is known to the person skilled in the art that the lifetime of OLEDs typically decreases with falling emitter concentration.

An excellent improvement in the lifetime with the same component efficiency and component voltage with an emitter concentration of 12% of a green emitter in the EML is obtained through the specific combination of a compound of the formula (1), represented by compound L2, with a compound of the formula (2), represented by compound B14 (BisCbz1), see Example E1 according to the invention, or with compound B3 (BisCbz2) in Example E3 according to the invention. Even with a lower emitter concentration of only 7% in the EML, the lifetime is still significantly improved compared with the prior art (Examples E2 and E4).

This improvement in the lifetime by a factor greater than 4 with comparable component voltage and comparable or improved component efficiency can preferably be achieved through the combination according to the invention of the compounds of the formula (1), as described above, with compounds of the formula (2), as described above, where n denotes 1 and Z has a meaning indicated above or a preferably indicated meaning, with emitter concentrations of 2 to 15% by weight in the emission layer.

This advantage is demonstrated as representative for compounds of the formula (1) through the use of compound L2 with the biscarbazole B14 (abbreviated to BisCbz1) in Example E1 with an emitter concentration of 12%.

Even with a lower emitter concentration of only 7% in the EML, at which the lifetime of an OLED typically drops, the lifetimes achieved of the combinations according to the invention are still significantly improved compared with the prior art. This is demonstrated as representative for compounds of the formula (1) through the use of compound L2 with the biscarbazole B14 (abbreviated to BisCbz1) in Example E2 with an emitter concentration of 7%.

The difference from Comparative Examples V1 and V2 lies in the electronic structure of the substituent Ar₁ or Ar₂ or the substituent R¹ in the biscarbazole of the formula (2), which carry very electron-rich heteroaromatic ring systems having 6 aromatic ring atoms and 3 nitrogen atoms. The person skilled in the art could not have foreseen that the lower electronic density of the biscarbazoles of the formula (2) selected in accordance with the invention causes an improved vapour-deposition behaviour and consequently results in an improvement in the lifetime of electronic devices, in particular OLEDs, by a factor greater than 4.

In contrast to the composition comprising a lactam and the biscarbazole,

from WO 2013/064206, the compositions have greater thermal stability and are less sensitive to crystallisation.

The compositions according to the invention are very highly suitable for use in an emission layer and exhibit improved performance data, in particular for the lifetime, compared with compounds from the prior art, as described above.

The compositions according to the invention can be processed easily and are therefore very highly suitable for mass production in commercial use.

The compositions according to the invention can be premixed and vapour-deposited from a single material source, so that an organic layer having a uniform distribution of the components used can be produced in a simple and rapid manner.

These above-mentioned advantages are not accompanied by an impairment of the other electronic properties of an electronic device.

It should be pointed out that variations of the embodiments described in the present invention fall within the scope of this invention. Each feature disclosed in the present invention can, unless this is explicitly excluded, be replaced by alternative features which serve the same, an equivalent or a similar purpose. Thus, each feature disclosed in the present invention is, unless stated otherwise, to be regarded as an example of a generic series or as an equivalent or similar feature.

All features of the present invention can be combined with one another in any way, unless certain features and/or steps are mutually exclusive. This applies, in particular, to preferred features of the present invention. Equally, features of non-essential combinations can be used separately (and not in combination).

The teaching regarding technical action disclosed with the present invention can be abstracted and combined with other examples.

The invention is explained in greater detail by the following examples without wishing to restrict it thereby.

General Methods:

Determination of Orbital Energies and Electronic States

The HOMO and LUMO energies and the triplet level and singlet levels of the materials are determined via quantum-chemical calculations. To this end, the “Gaussian09, Revision D.01” software package (Gaussian Inc.) is used in the present application. For the calculation of organic substances without metals (denoted by “org.” method), firstly a geometry optimisation is carried out using the semi-empirical method AM1 (Gaussian input line “# AM1 opt”) with charge 0 and multiplicity 1. This is followed by an energy calculation (single point) for the electronic ground state and triplet level on the basis of the optimised geometry. The TDDFT (time dependent density functional theory) method B3PW91 with the 6-31G(d) base set (Gaussian input line “# B3PW91/6-31G(d) td=(50-50,nstates=4)”) is used here (charge 0, multiplicity 1). For organometallic compounds (denoted by “org.-m” method), the geometry is optimised using the Hartree-Fock method and the LanL2 MB base set (Gaussian input line “# HF/LanL2 MB opt”) (charge 0, multiplicity 1). The energy calculation is carried out, as described above, analogously to that of the organic substances, with the difference that the “LanL2DZ” base set is used for the metal atom and the “6-31G(d)” base set is used for the ligands (Gaussian input line “# B3PW91/gen pseudo=lanl2 td=(50-50,nstates=4)”). The energy calculation gives the HOMO as the last orbital occupied by two electrons (Alpha occ. eigenvalues) and LUMO as the first unoccupied orbital (alpha virt. eigenvalues) in hartree units, where HEh and LEh stand for the HOMO energy in hartree units and the LUMO energy in hartree units respectively. The HOMO and LUMO values in electron volts calibrated with reference to cyclic voltammetry measurements are determined thereform as follows:

HOMO (eV)=(HEh*27.212)*0.8308−1.118;

LUMO (eV)=(LEh*27.212)*1.0658−0.5049.

The triplet state T1 of a material is defined as the relative excitation energy (in eV) of the triplet state having the lowest energy which arises from the quantum-chemical energy calculation.

The singlet level S1 is defined as the relative excitation energy (in eV) of the singlet state having the second lowest energy which arises from the quantum-chemical energy calculation.

The singlet state of lowest energy is called S0.

The method described herein is independent of the software package used and always gives the same results. Examples of frequently used programs for this purpose are “Gaussian09” (Gaussian Inc.) and Q-Chem 4.1 (Q-Chem, Inc.). In the present application, the “GaussianO9, Revision D.01” software package is used for the calculation of the energies.

EXAMPLE 1: PRODUCTION OF THE OLEDS

The use of the material combinations according to the invention in OLEDs is presented in Examples E1, E2, E3 and E4 below (see Table 7).

Pretreatment for Examples E1-E4

Glass plates coated with structured ITO (indium tin oxide) in a thickness of 50 nm are, before coating, treated firstly with an oxygen plasma, followed by an argon plasma. These plasma-treated glass plates form the substrates to which the OLEDs are applied.

The OLEDs have basically the following layer structure: substrate/hole-injection layer (HIL)/hole-transport layer (HTL)/electron-blocking layer (EBL)/emission layer (EML)/optional hole-blocking layer (HBL)/electron-transport layer (ETL)/optional electron-injection layer (EIL) and finally a cathode. The cathode is formed by an aluminium layer with a thickness of 100 nm. The precise structure of the OLEDs is shown in Table 7. The materials required for the production of the OLEDs are shown in Table 8. The data of the OLEDs are listed in Table 9. Examples V1 to V7 are comparative examples in accordance with WO 2014/094964, Examples E1, E2, E3 and E4 show data of OLEDs according to the invention.

All materials are applied by thermal vapour deposition in a vacuum chamber. The emission layer here always consists of at least one matrix material (host material), in the sense of the invention at least two matrix materials, and an emitting dopant (emitter), which is admixed with the matrix material or matrix materials in a certain proportion by volume by co-evaporation. An expression such as CbzT1:BisC1:TEG1 (45%:45%:10%) here means that material CbzT1 is present in the layer in a proportion by volume of 45%, BisC1 is present in the layer in a proportion of 45% and TEG1 is present in the layer in a proportion of 10%. Analogously, the electron-transport layer may also consist of a mixture of two materials.

The OLEDs are characterised by standard methods. For this purpose, the electroluminescence spectra, the current efficiency (CE, gemessen in cd/A) and the external quantum efficiency (EQE, measured in %) as a function of the luminous density, calculated from current/voltage/luminous density characteristic lines assuming Lambert emission characteristics, and the lifetime are determined. The electroluminescence spectra are determined at a luminous density of 1000 cd/m² and the CIE 1931 x and y colour coordinates are calculated therefrom. The term U1000 in Table 9 denotes the voltage required for a luminous density of 1000 cd/m². CE1000 and EQE1000 denote the current efficiency and external quantum efficiency respectively that are achieved at 1000 cd/m².

The lifetime LT defines the time after which the luminous density drops from the initial luminous density to a certain proportion L1 on operation at a constant current density j₀. An expression L1=80% in Table 9 means that the lifetime indicated in column LT corresponds to the time after which the luminous density drops to 80% of its initial value.

Use of Mixtures According to the Invention in OLEDs

The material combinations according to the invention can be employed in the emission layer in phosphorescent OLEDs. The combination according to the invention of compound L2 with BisCbz1 (corresponding to compound B14) is employed in Examples E1 and E2 as matrix material in the emission layer. The combination according to the invention of compound L2 with BisCbz2 (corresponding to compound B3) is employed in Examples E3 and E4 as matrix material in the emission layer.

TABLE 7 Structure of the OLEDs HIL HTL EBL EML HBL ETL EIL Ex. Thickness Thickness Thickness Thickness Thickness Thickness Thickness V1 SpA1 HATCN SpMA1 L1:CbzT2:TEG1 IC1 ST2:LiQ (50%:50%) — 70 nm 5 nm 90 nm (45%:45%:10%) 40 nm 5 nm 25 nm V2 SpA1 HATCN SpMA1 L1:CbzT3:TEG1 IC1 ST2:LiQ (50%:50%) — 70 nm 5 nm 90 nm (45%:45%:10%) 40 nm 5 nm 25 nm V3 HATCN — SpMA3 L2:CbzT3:TEY2 — ST1 LiQ 5 nm 90 m (45%:45%:10%) 30 nm 40 nm 3 nm V4 HATCN — SpMA3 L2:IC6:TEY2 — ST1 LiQ 5 nm 90 m (45%:45%:10%) 30 nm 40 nm 3 nm V5 HATCN — SpMA5 L2:IC6:TEY2 — ST1 LiQ 5 nm 90 m (45%:45%:10%) 30 nm 40 nm 3 nm V6 HATCN — SpMA4 L2:IC6:TEY2 — ST1 LiQ 5 nm 90 m (45%:45%:10%) 30 nm 40 nm 3 nm V7 HATCN — SpMA6 L2:IC6:TEY2 — ST1 LiQ 5 nm 90 m (45%:45%:10%) 30 nm 40 nm 3 nm E1 HATCN SpMA1 SpMA2 L2:BisCbz1:TEG2 ST2 ST2:LiQ (50%:50%) LiQ 5 nm 215 nm 20 nm (66%:22%:12%) 30 nm 10 nm 30 nm 1 nm E2 HATCN SpMA1 SpMA2 L2:BisCbz1:TEG2 ST2 ST2:LiQ (50%:50%) LiQ 5 nm 215 nm 20 nm (63%:30%:7%) 30 nm 10 nm 30 nm 1 nm E3 HATCN SpMA1 SpMA2 L2:BisCbz2:TEG2 ST2 ST2:LiQ (50%:50%) LiQ 5 nm 215 nm 20 nm (44%:44%:12%) 30 nm 10 nm 30 nm 1 nm E4 HATCN SpMA1 SpMA2 L2:BisCbz2:TEG2 ST2 ST2:LiQ (50%:50%) LiQ 5 nm 215 nm 20 nm (58%:35%:7%) 30 nm 10 nm 30 nm 1 nm

TABLE 8 Structural formulae of the materials for OLEDs

TABLE 9 Data of the OLEDs CIE x/y at U1000 CE1000 EQE 1000 1000 J₀ L1 LT Ex. (V) (cd/A) (%) cd/m² (mA/cm²) (%) (h) V1 3.5 53 14.8 0.32/0.63 20 80 190 V2 3.4 55 15.4 0.33/0.63 20 80 215 V3 3.0 86 25.3 0.44/0.55 50 90 130 V4 2.7 84 24.4 0.44/0.55 50 90 190 V5 2.9 83 14.6 0.44/0.55 50 90 225 V6 3.0 86 25.4 0.44/0.55 50 90 140 V7 2.9 80 23.5 0.44/0.55 50 90 180 E1 3.4 64 17.1 0.34/0.63 20 80 1000 E2 3.3 57 15.3 0.34/0.63 20 80 955 E3 3.3 66 18.0 0.31/0.64 20 80 790 E4 3.3 74 20.2 0.31/0.64 20 80 395

Following the model of Examples E1 to E4, the combination of further lactams (right-hand column Table 10) with biscarbazoles (left-hand column Table 10) and phosphorescent emitters gives OLEDs having excellent performance data, which demonstrates the broad applicability of the material combination according to the invention.

TABLE 10 Structural formulae for further material combinations Biscarbazoles (BisCbz)

B1

B1

B1

B1

B1

B1

B1

B2

B2

B2

B2

B2

B2

B2

B3

B3

B3

B3

B3

B3

B3 Lactams (L)

L6

L10

L21

L32

L33

L6

L10

L21

L32

L33

L6

L10

L21

L32

L33

EXAMPLE 2: SYNTHESIS OF COMPOUNDS L1 AND L2

Compound L1 is known from the literature and is prepared analogously to WO 2014/094964, Synthesis Example 1, pages 58 and 59.

Compound L2 is known from the literature and is prepared analogously to WO 2014/094964, Synthesis Example L8, pages 60 to 62.

EXAMPLE 3: SYNTHESIS OF COMPOUND B14

Compound B14 is known from the literature and is prepared analogously to WO 2010136109, Example 50, pages 133 and 134. 

1.-18. (canceled)
 19. A composition comprising at least one compound of the formula (1) and at least one compound of the formula (2)

where the following applies to the symbols and indices used: X is on each occurrence, identically or differently, CR or N; V is a bond, C(R⁰)₂, O or S; v is 0 or 1; X₂ is on each occurrence, identically or differently, CR¹ or N; Z is C(R⁰)₂, NR¹, O or S; n is 0 or 1; Ar₁ and Ar₂ are in each case, independently of one another, an aromatic ring system having 6 to 40 aromatic ring atoms or a heteroaromatic ring system having 10 to 40 aromatic ring atoms, which may be substituted by one or more radicals R³; R⁰ is on each occurrence, identically or differently, a straight-chain or branched alkyl group having 1 to 4 C atoms or both R⁰ form a monocyclic or polycyclic, aliphatic, aromatic or heteroaromatic ring system, which may be substituted by one or more radicals R²; R is selected on each occurrence, identically or differently, from the group consisting of H, D, F, Cl, Br, I, CN, NO₂, N(Ar)₂, N(R²)₂, C(═O)Ar, C(═O)R², P(═O)(Ar)₂, P(Ar)₂, B(Ar)₂, Si(Ar)₃, Si(R²)₃, a straight-chain alkyl, alkoxy or thioalkyl group having 1 to 20 C atoms or a branched or cyclic alkyl, alkoxy or thioalkyl group having 3 to 20 C atoms or an alkenyl group having 2 to 20 C atoms, which may in each case be substituted by one or more radicals R², where one or more non-adjacent CH₂ groups may be replaced by R²C═CR², Si(R²)₂, C═O, C═S, C═NR², P(═O)(R²), SO, SO₂, NR², O, S or CONR² and where one or more H atoms may be replaced by D, F, Cl, Br, I, CN or NO₂, an aromatic or heteroaromatic ring system having 5 to 40 aromatic ring atoms, which may in each case be substituted by one or more radicals R², or an aryloxy or heteroaryloxy group having 5 to 40 aromatic ring atoms, which may be substituted by one or more radicals R², or an aralkyl or heteroaralkyl group having 5 to 40 aromatic ring atoms, which may be substituted by one or more radicals R²; two substituents R which are bonded to the same carbon atom or to adjacent carbon atoms may optionally form a monocyclic or polycyclic, aliphatic, aromatic or heteroaromatic ring system, which may be substituted by one or more radicals R²; R¹ is selected on each occurrence, identically or differently, from the group consisting of H, D, F, Cl, Br, I, CN, NO₂, N(Ar)₂, N(R²)₂, C(═O)Ar, C(═O)R², P(═O)(Ar)₂, P(Ar)₂, B(Ar)₂, Si(Ar)₃, Si(R²)₃, a straight-chain alkyl, alkoxy or thioalkyl group having 1 to 20 C atoms or a branched or cyclic alkyl, alkoxy or thioalkyl group having 3 to 20 C atoms or an alkenyl group having 2 to 20 C atoms, which may in each case be substituted by one or more radicals R², where one or more non-adjacent CH₂ groups may be replaced by R²C═CR², Si(R²)₂, C═O, C═S, C═NR², P(═O)(R²), SO, SO₂, NR², O, S or CONR² and where one or more H atoms may be replaced by D, F, Cl, Br, I, CN or NO₂, an aromatic or heteroaromatic ring system having 5 to 40 aromatic ring atoms, which may in each case be substituted by one or more radicals R², or an aryloxy or heteroaryloxy group having 5 to 40 aromatic ring atoms, which may be substituted by one or more radicals R², or an aralkyl or heteroaralkyl group having 5 to 40 aromatic ring atoms, which may be substituted by one or more radicals R²; R² is selected on each occurrence, identically or differently, from the group consisting of H, D, F, Cl, Br, I, CN, NO₂, N(Ar)₂, NH₂, N(R³)₂, C(═O)Ar, C(═O)H, C(═O)R³, P(═O)(Ar)₂, a straight-chain alkyl, alkoxy or thioalkyl group having 1 to 40 C atoms or a branched or cyclic alkyl, alkoxy or thioalkyl group having 3 to 40 C atoms or an alkenyl or alkynyl group having 2 to 40 C atoms, which may in each case be substituted by one or more radicals R³, where one or more non-adjacent CH₂ groups may be replaced by HC═CH, R³C═CR³, C═C, Si(R³)₂, Ge(R³)₂, Sn(R³)₂, C═O, C═S, C═Se, C═NR³, P(═O)(R³), SO, SO₂, NH, NR³, O, S, CONH or CONR³ and where one or more H atoms may be replaced by D, F, Cl, Br, I, CN or NO₂, an aromatic or heteroaromatic ring system having 5 to 60 aromatic ring atoms, which may in each case be substituted by one or more radicals R³, or an aryloxy or heteroaryloxy group having 5 to 60 aromatic ring atoms, which may be substituted by one or more radicals R³, or a combination of these systems, where two or more adjacent substituents R² may optionally form a monocyclic or polycyclic, aliphatic, aromatic or heteroaromatic ring system, which may be substituted by one or more radicals R³; R³ is selected on each occurrence, identically or differently, from the group consisting of H, ID, F, CN, an aliphatic hydrocarbon radical having 1 to 20 C atoms or an aromatic ring system having 6 to 30 ring atoms or a heteroaromatic ring system having 10 to 30 ring atoms, in which one or more H atoms may be replaced by D, F, Cl, Br, I or CN and which may be substituted by one or more alkyl groups, each having 1 to 4 carbon atoms; two or more adjacent substituents R³ may form a mono- or polycyclic, aliphatic ring system with one another; Ar is on each occurrence, identically or differently, an aromatic or heteroaromatic ring system having 5 to 30 aromatic ring atoms, which may be substituted by one or more non-aromatic radicals R³; two radicals Ar which are bonded to the same N atom, P atom or B atom may also be bridged to one another by a single bond or a bridge selected from N(R³), C(R³)₂, O or S.
 20. The composition according to claim 19, wherein the compound of the formula (1) corresponds to the formula (1a),

where the symbols and indices used have a meaning as in claim
 19. 21. The composition according to claim 19, wherein the compound of the formula (2) corresponds to the formula (2a),

where the symbols and indices used have a meaning as in claim 19, q and t in each case, independently of one another, denote 0, 1, 2, 3 or 4 and r and s in each case, independently of one another, denote 0, 1, 2 or
 3. 22. The composition according to claim 19, wherein one of the substituents Ar₁ and Ar₂ denotes an aromatic ring system having 6 to 40 aromatic ring atoms or a heteroaromatic ring system having 10 to 40 aromatic ring atoms, which may be substituted by one or more radicals R³, and the other substituent denotes an aromatic ring system having 6 to 40 aromatic ring atoms, which may be substituted by one or more radicals R³.
 23. The composition according to claim 19, wherein the substituents Ar₁ and Ar₂ in each case, independently of one another, denote an aromatic ring system having 6 to 40 aromatic ring atoms, which may be substituted by one or more radicals R³.
 24. The composition according to claim 19, wherein the composition comprises at least one further compound selected from the group consisting of hole-injection materials, hole-transport materials, hole-blocking materials, wide bandgap materials, fluorescent emitters, phosphorescent emitters, host materials, electron-blocking materials, electron-transport materials and electron-injection materials, n-dopants and p-dopants.
 25. A formulation comprising a composition according to claim 19 and at least one solvent.
 26. An organic electronic device containing at least one composition according to claim
 19. 27. The device according to claim 26, wherein the device is selected from the group of organic integrated circuits (OICs), organic field-effect transistors (OFETs), organic thin-film transistors (OTFTs), organic electroluminescent devices, organic solar cells (OSCs), organic optical detectors and organic photoreceptors.
 28. The device according to claim 26, wherein the device is an electroluminescent device selected from organic light-emitting transistors (OLETs), organic field-quench devices (OFQDs), organic light-emitting electrochemical cells (OLECs, LECs, LEECs), organic laser diodes (O-lasers) and organic light-emitting diodes (OLEDs).
 29. The device according to claim 26, wherein the device contains the composition in an emission layer (EML), in an electron-transport layer (ETL), in an electron-injection layer (EIL) and/or in a hole-blocking layer (HBL).
 30. The device according to claim 26, wherein the device contains the composition in the emission layer together with a phosphorescent emitter.
 31. A process for the production of the device according to claim 26, which comprises applying at least one organic layer comprising the composition by gas-phase deposition or from solution.
 32. The process according to claim 31, wherein the at least one compound of the formula (1) and the at least one compound of the formula (2) are deposited from the gas phase successively or simultaneously from at least two material sources, optionally with further materials, and form the organic layer.
 33. The process according to claim 31, wherein the composition according to claim 19 is utilised as material source for the gas-phase deposition and forms the organic layer.
 34. The process according to claim 31, wherein the formulation according to claim 25 is used in order to apply the organic layer. 